OVERVIEW



The following discussion should be read in conjunction with the unaudited
condensed financial statements and notes thereto set forth in Item 1 of this
Quarterly Report on Form 10-Q and the audited financial statements and notes
thereto included in our Annual Report on Form 10-K for the year ended December
31, 2019 (the "2019 Form 10-K").

Except for the historical information contained herein, the matters discussed in
this Quarterly Report on Form 10-Q may be deemed to be forward-looking
statements that involve risks and uncertainties.  We make such forward-looking
statements pursuant to the safe harbor provisions of the Private Securities
Litigation Reform Act of 1995 and other federal securities laws.  In this
Quarterly Report on Form 10-Q, words such as "believe", "estimate", "expect",
"anticipate", "will", "may", "intend" and other similar expressions, are
intended to identify forward-looking statements.  We caution that
forward-looking statements are based largely on our expectations and are subject
to a number of known and unknown risks and uncertainties that are subject to
change based on factors that are, in many instances, beyond our control.  Actual
results, performance or achievements may differ materially from those
contemplated, expressed or implied by the forward-looking statements.

Although we believe that the expectations reflected in our forward-looking statements are reasonable as of the date we make them, actual results could differ materially from those currently anticipated due to a number of factors, including risks relating to:

• uncertainties about the Merger (as defined below), including but not limited to

our ability to close the Merger, our ability to obtain adequate liquidity to

fund our operations, meet our obligations, and continue as a going concern if

the Merger is not completed, and that the Merger may not enhance shareholder

value and may create a distraction or uncertainty that may adversely affect our

operating results, business, or investor perceptions;

• our ability to control and correctly estimate our operating expenses, our

estimated warrant liabilities and our expenses associated with the Merger,

including litigation expenses, which could result in us having significantly

less net cash than currently anticipated, which may prevent us from

consummating the Merger or result in our stockholders owning significantly less

of the combined company than currently estimated;

• conditions to payment under the CVRs may not be met and the CVRs may never

deliver any value to our stockholders;

• uncertainties about the paths of our programs and our ability to evaluate and

identify a path forward for those programs, particularly given the constraints


   we have as a small company with limited financial, personnel and other
   operating resources;


• the impact of the COVID-19 pandemic on the economy, our industry, and our


   financial condition and results of operations, as well as our ability to
   consummate the Merger;


• our understandings and beliefs regarding the role of certain biological


   mechanisms and processes in cancer;



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• our product candidates being in early stages of development, including in


   preclinical development;



• our ability to successfully and timely complete clinical trials for our drug

candidates in clinical development;

• uncertainties related to the timing, results and analyses related to our drug

candidates in preclinical development;

• our ability to obtain the necessary U.S. and international regulatory approvals


   for our drug candidates;



• our reliance on third-party contract research organizations and other

investigators and collaborators for certain research and development services;

• our ability to maintain or engage third-party manufacturers to manufacture,

supply, store and distribute supplies of our drug candidates for our clinical


   trials;



• our ability to form strategic alliances and partnerships with pharmaceutical

companies and other partners for development, sales and marketing of certain of


   our product candidates;



• demand for and market acceptance of our drug candidates;

• the scope and validity of our intellectual property protection for our drug

candidates and our ability to develop our candidates without infringing the

intellectual property rights of others;

• our lack of profitability and the need for additional capital to operate our


   business; and



• other risks and uncertainties, including those set forth herein and in the 2019

Form 10-K under the caption "Risk Factors" and those detailed from time to time

in our filings with the Securities and Exchange Commission.

These forward-looking statements are made only as of the date hereof, and we undertake no obligation to update or revise the forward-looking statements, whether as a result of new information, future events or otherwise.



We are a clinical stage biopharmaceutical company that has been focused on the
development of innovative therapies to improve patient outcomes in cancers that
are difficult to treat. Our pipeline has featured two clinical-stage product
candidates and additional compounds in preclinical development.

• RX-3117 is a novel, investigational oral, small molecule nucleoside compound.

Once intracellularly activated (phosphorylated) by the enzyme UCK2, it is

incorporated into the DNA or RNA of cells and inhibits both DNA and RNA

synthesis, which induces apoptotic cell death of tumor cells. RX-3117 has been

the subject of a Phase 2a clinical trial in combination with Celgene's

ABRAXANE® (paclitaxel protein-bound particles for injectable suspension) as a

first-line treatment in patients newly diagnosed with metastatic pancreatic

cancer. The trial reached its target enrollment in February 2019. As of July

24, 2019, an overall response rate of 23% had been observed in 40 patients that

had at least one scan on treatment. Preliminary and unaudited data indicates

that the median progression free survival for patients in the study is


   approximately 5.4 months.  Complete data from the trial is expected to be
   available in 2020.  We do not plan to conduct or sponsor any additional trials
   with RX-3117.



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On March 10, 2020, we amended our collaboration and license agreement (as
amended, the "License and Assignment Agreement") with BioSense Global LLC
("BioSense") to advance the development and commercialization of RX-3117 for all
human uses in the Republic of Singapore, China, Hong Kong, Macau, and Taiwan
(the "Territory"). Under the terms of the License and Assignment Agreement, upon
payment in full of an upfront payment, we will grant BioSense an exclusive
license to develop and commercialize pharmaceutical products containing RX-3117
as a single agent for all human uses in the Territory and assign and transfer to
BioSense all of our patents and patent applications related to RX-3117 in the
Territory. The upfront payment consists of an aggregate of $1,650,000, of which
$1,550,000 has been received to date. Under the License and Assignment
Agreement, we are eligible to receive milestone payments in an aggregate of up
to $84.5 million upon the achievement of development, regulatory and commercial
goals and will also be eligible to receive tiered royalties in the mid-single
digits to low tens on annual net sales in the Territory.

• RX-5902 is a potential first-in-class small molecule modulator of the

Wnt/beta-catenin pathway which plays a key role in cancer cell proliferation

and tumor growth. In August 2018, we entered into a Clinical Trial

Collaboration and Supply Agreement (the "Collaboration Agreement") with Merck

Sharp & Dohme B.V. ("Merck") to evaluate the combination of RX-5902 and Merck's

anti-PD-1 therapy, KEYTRUDA® (pembrolizumab) in a Phase 2 trial in patients

with metastatic triple negative breast cancer ("TNBC"). On April 7, 2020, we

notified Merck that we were terminating the Collaboration Agreement, effective

immediately, in connection with our determination to discontinue development of

RX-5902 for the treatment of TNBC. We do not plan to conduct or sponsor any

additional trials with RX-5902.

• RX-0301 is a potential best-in-class, potent inhibitor of the synthesis of the

protein kinase Akt-1, which we believe plays a critical role in cancer cell

proliferation, survival, angiogenesis, metastasis, and drug resistance.

RX-0301 is currently in preclinical development by Zhejiang HaiChang

Biotechnology Co., Ltd. ("HaiChang") as a nano-liposomal formulation of RX-0201

(Archexin®) using HaiChang's proprietary QTsome™ technology. On February 8,

2020, we entered into an exclusive license agreement with HaiChang (the

"HaiChang License Agreement") pursuant to which we granted HaiChang an

exclusive (even as to us), royalty-bearing, sublicensable worldwide license to

research, develop and commercialize RX-0201 and RX-0301. The HaiChang License

Agreement supersedes a prior agreement with HaiChang to develop RX-0301 under

which HaiChang was to conduct certain preclinical and clinical activities


   through completion of a Phase 2a proof-of-concept clinical trial in
   hepatocellular carcinoma.



Merger Agreement

In September 2019, we commenced a process to explore and evaluate strategic
alternatives to enhance stockholder value, and had engaged Oppenheimer & Co.
Inc. as our financial advisor to assist us in this process. In June 2020, we
entered into an Agreement and Plan of Merger and Reorganization (as amended, the
"Merger Agreement") with Razor Merger Sub, Inc., a Delaware corporation and our
wholly owned subsidiary ("Merger Sub") and Ocuphire Pharma, Inc., a Delaware
corporation ("Ocuphire"), pursuant to which our wholly owned subsidiary, Merger
Sub, will merge with and into Ocuphire, with Ocuphire surviving as our wholly
owned subsidiary in an all-stock transaction (the "Merger"). Pursuant to the
Merger Agreement, at the effective time of the Merger (the "Effective Time"), we
will also enter into a CVR Agreement, pursuant to which, for each share of our
common stock held, our stockholders of record as of immediately prior to the
Effective Time will receive one contingent value right ("CVR").  Refer to Note
2- Merger Agreement and Pre-Merger Financing to our condensed financial
statements included in Part I "Financial Information", Item 1 "Financial
Statements" of this Quarterly Report on Form 10-Q for further information. The
discussion below excludes any impact that may result from the Merger.  The
Merger has been approved by the boards of directors of both companies and is
expected to close in the second half of 2020, subject to approval by our
stockholders and Ocuphire's stockholders as well as certain other closing
conditions. The total fees and costs of the proposed Merger are expected to be
material to our results of operations in 2020. Following the Merger, the
combined company will be a clinical-stage ophthalmic biopharmaceutical company
focused on developing and commercializing therapies for the treatment of several
eye disorders.

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Although we have entered into the Merger Agreement and intend to consummate the
Merger, there is no assurance that we will be able to successfully consummate
the Merger on a timely basis, or at all. If, for any reason, the Merger does not
close, our board of directors may elect to, among other things, attempt to
complete another strategic transaction like the Merger, attempt to sell or
otherwise dispose of our various assets, resume our research and development
activities and continue to operate our business or dissolve and liquidate our
assets. If we decide to dissolve and liquidate our assets, we would be required
to pay all of our debts and contractual obligations, and to set aside certain
reserves for potential future claims, and there can be no assurances as to the
amount or timing of available cash left, if any, to distribute to stockholders
after paying our debts and other obligations and setting aside funds for
reserves. If we were to continue our business, we would need to raise a
substantial amount of cash to fund ongoing operations and future development
activities for our existing product candidates and any new product candidates
that we acquire.

Pre-Merger Financing

Securities Purchase Agreement



On June 29, 2020, Ocuphire, us and certain institutional healthcare investors,
accredited investors and directors and officers of Ocuphire (the "Investors")
entered into a Securities Purchase Agreement (the "Securities Purchase
Agreement"), which amended and restated in its entirety the prior securities
purchase agreement among the same parties dated June 17, 2020 (the "Initial
Securities Purchase Agreement"). The Securities Purchase Agreement that was
entered into on June 29, 2020 was substantially similar to the Initial
Securities Purchase Agreement, except (i) the number of Additional Shares (as
defined below) to be deposited into escrow was increased from two times the
number of Initial Shares (as defined below) of Ocuphire common stock to three
times the number of Initial Shares of Ocuphire common stock, (ii) the
Registration Rights Agreement, dated, June 17, 2020, by and among us and the
Investors (the "Registration Rights Agreement") was terminated in its entirety,
and (iii) certain of our obligations were revised to reflect termination of the
Registration Rights Agreement.

Pursuant to the Securities Purchase Agreement, the Investors agreed to invest a
total of $21.15 million in cash (the "Purchase Price" and the financing
arrangement described herein, the "Pre-Merger Financing") to fund the combined
company following the consummation of the Merger. In return, based on an agreed
upon pre-money valuation of the combined company following the Merger (the
"combined company") of $120 million, Ocuphire will issue an amount of shares of
Ocuphire common stock (the "Initial Shares") to the Investors, which shares will
be exchangeable in the Merger for approximately 15% of the Pre-Merger Financing
Fully Diluted Shares (as defined below). In addition, (i) Ocuphire will deposit
three times the number of Initial Shares of Ocuphire common stock (the
"Additional Shares," and together with the Initial Shares, the "Pre-Merger
Financing Shares") into escrow with an escrow agent for the benefit of the
Investors, to be exchanged for shares of our common stock in the Merger, and to
be delivered, in whole or in part, based on the formula set forth below, out of
escrow to the Investors if 85% of the average of the five lowest volume-weighted
average trading prices of a share of our common stock on The Nasdaq Stock Market
("Nasdaq") during the first ten trading days (or earlier, at the election of any
Investor) immediately following the closing date of the Pre-Merger Financing
(which closing date will be the same date as the Closing) is lower than the
effective price per share paid by the Investors for the Converted Initial Shares
(as defined below), and (ii) on the tenth trading day following the closing date
of the Pre-Merger Financing (the "warrant closing date"), we will issue to the
Investors (x) Series A warrants to purchase shares of our common stock, as
further described below (the "Series A Warrants"), and (y) Series B warrants to
purchase shares of our common stock, as further described below (the "Series B
Warrants," together with the Series A Warrants,  the "Investor Warrants" and,
together with the Pre-Merger Financing Shares, the "Purchased Securities").

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"Pre-Merger Financing Fully Diluted Shares" means the "fully-diluted"
post-Merger outstanding shares of our common stock, which amount (i) includes
all shares of our common stock that may be issued pursuant to in-the-money
options, warrants or convertible securities, and (ii) with respect to new
warrants issued after the date of the Initial Securities Purchase Agreement in
exchange for existing warrants shall include (A) all shares of our common stock
that are subject to each new warrant that is in-the-money as of the date of
issuance of such new warrant and (B) 0.5 times the number of shares of our
common stock that may be issued pursuant to such out-of-the-money new warrant
that is out-of-the-money as determined based on the closing sale price of our
common stock immediately following the issuance of such warrant, and (iii)
excludes all other out-of-the-money options, warrants or convertible securities
of ours.

As a result of the Merger, at the Effective Time, the Initial Shares will
automatically be converted into the right to receive a number of shares (the
"Converted Initial Shares") of our common stock equal to the number of Initial
Shares multiplied by the Exchange Ratio. Further, at the Effective Time, the
Additional Shares placed into escrow with the escrow agent will automatically be
converted into the right to receive a number of shares (the "Converted
Additional Shares") of our common stock equal to the number of Additional Shares
multiplied by the Exchange Ratio. The number of Converted Additional Shares
deliverable out of escrow to each Investor will be equal to the lesser of (I)
the number of Converted Additional Shares issued in exchange for the Additional
Shares deposited in the Investor's escrow account and (II) the number determined
on or prior to the warrant closing date by subtracting (i) the number of
Converted Initial Shares issued to the Investor from (ii) the quotient
determined by dividing (a) the pro rata portion of the Purchase Price paid by
the Investor by (b) 85% of the average of the five lowest volume-weighted
average trading prices of a share of our common stock on Nasdaq during the first
ten trading days (or earlier at the election of any Investor) immediately
following the Closing, subject to the Floor Price (as defined below). Any
Converted Additional Shares not deliverable to the Investors as of the warrant
closing date based on the foregoing formula will be returned to us as treasury
shares and cancelled. No Converted Additional Shares will be deliverable out of
escrow if the foregoing formula results in a negative number. The lower of (x)
the effective initial purchase price per Converted Initial Share and (y) the
number obtained by the formula in clause (b) above, subject to the Floor Price,
is called the "Final Purchase Price." Notwithstanding the foregoing, no
Converted Additional Shares will be delivered to Investors from escrow to the
extent such delivery would result in such Investor, together with its affiliates
and any other person whose beneficial ownership of our common stock would be
aggregated with such Investor for purposes of Section 13(d) of the Exchange Act,
beneficially owning in excess of 4.99% or 9.99% of our outstanding common stock
(including the Converted Additional Shares so delivered). In the event that we
fail to timely deliver any of the Converted Initial Shares or Converted
Additional Shares then we shall be obligated to pay the affected Investor on
each day while such failure is continuing an amount equal to 1.5% of the market
value of the undelivered shares determined using any trading price of our common
stock selected by the holder while the failure is continuing and if an affected
Investor purchases shares of our common stock in connection with such failure
("Buy-In Shares"), then we must, at such Investor's discretion, reimburse such
Investor for the cost of such Buy-In Shares or deliver the owed shares and
reimburse the Investor for the difference between the price such Investor paid
for the Buy-In Shares and the market price of such shares, measured at any time
of such Investor's choosing while the delivery failure was continuing.

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Pursuant to the Securities Purchase Agreement, at any time during the period
commencing from the six month anniversary of the closing date of the Pre-Merger
Financing and ending at such time that all of the shares of our common stock
issued or issuable in the Pre-Merger Financing, if a registration statement is
not available for the resale of such shares, may be sold without restriction or
limitation pursuant to Rule 144 of the Securities Act of 1933, as amended (the
"Securities Act") and without the requirement to be in compliance with Rule
144(c)(1), if we (i) shall fail for any reason to satisfy the requirements of
Rule 144(c)(1) under the Securities Act, including, without limitation, the
failure to satisfy the current public information requirements under Rule 144(c)
under the Securities Act or (ii) has ever been an issuer described in Rule
144(i)(1)(i) under the Securities Act or becomes such an issuer in the future,
and we shall fail to satisfy any condition set forth in Rule 144(i)(2) under the
Securities Act (each, a "Public Information Failure"), then we shall pay to each
holder of Purchased Securities an amount in cash equal to 2.0% of such holder's
pro rata portion of the Purchase Price on the day of such Public Information
Failure and on every thirtieth day thereafter until the earlier of (i) the date
such Public Information Failure is cured and (ii) the date on which such Public
Information Failure no longer prevents a holder of Purchased Securities from
selling such Purchased Securities pursuant to Rule 144 under the Securities Act
without any restrictions or limitations.

The Securities Purchase Agreement contains customary representations and
warranties of Ocuphire, us and the Investors. Each party's obligation to
consummate the transactions contemplated by the Securities Purchase Agreement is
subject to the satisfaction or waiver of certain conditions, including the
satisfaction or waiver of each of the conditions precedent to the Closing
contained in the Merger Agreement, other than any conditions precedent relating
to consummation of the Pre-Merger Financing.

The Securities Purchase Agreement restricts us from filing a registration
statement or any amendment or supplement thereto, causing any registration
statement to be declared effective by the Securities and Exchange Commission
("SEC"), or granting any registration rights, in each case subject to certain
limited exceptions, until the date that is 90 days after the earlier of (i) such
time as all of the shares of our common stock issued or issuable in the
Pre-Merger Financing may be sold without restriction or limitation pursuant to
Rule 144, and (ii) the date that is six months following the closing of the
Pre-Merger Financing; provided that in the event of a Public Information
Failure, such date shall be such later date on which the Public Information
Failure is cured and no longer prevents the Investors from selling all shares of
our common stock issued or issuable in the Pre-Merger Financing (the 90th date
after such earlier date, the "Trigger Date").

Pursuant to the Securities Purchase Agreement, until 240 calendar days following
the closing of the Pre-Merger Financing, subject to certain exceptions, neither
Ocuphire nor we may (i) offer, sell, grant any option to purchase, or otherwise
dispose of any of its or its subsidiaries' debt, equity or equity equivalent
securities (any such offer, sale, grant, disposition or announcement being
referred to as a "Subsequent Placement"), or (ii) be party to any solicitations,
negotiations or discussions with regard to the foregoing.

Additionally, for one year following the closing of the Pre-Merger Financing,
Ocuphire, us and each of our respective subsidiaries shall be prohibited from
effecting or entering into an agreement to effect any Subsequent Placement
involving a transaction in which Ocuphire, us or any of their subsidiaries (i)
issues or sells any stock or securities convertible into or exercisable or
exchangeable for Ocuphire common stock or our common stock ("Convertible
Securities") either (a) at a conversion, exercise or exchange rate or other
price that is based upon and/or varies with the trading prices of or quotations
for the shares of Ocuphire common stock or our common stock at any time after
the initial issuance of such Convertible Securities, or (b) with a conversion,
exercise or exchange price that is subject to being reset at some future date
after the initial issuance of such Convertible Securities or upon the occurrence
of specified or contingent events directly or indirectly related to the business
of Ocuphire or us or the market for Ocuphire common stock or our common stock,
other than pursuant to a customary "weighted average" anti-dilution provision or
(ii) enters into any agreement (including, without limitation, an equity line of
credit or an "at-the-market" offering) whereby Ocuphire, us or any of our
respective subsidiaries may sell securities at a future determined price (other
than standard and customary "preemptive" or "participation" rights); provided,
that we will be permitted to consummate "at the market" offerings at any time
after the later of (x) the date that is nine (9) months after the closing date
of the Pre-Merger Financing and (y) the Trigger Date.

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The Securities Purchase Agreement may be amended only by an instrument in
writing signed by Ocuphire, us and the Required Holders (as defined below). No
provision of the Securities Purchase Agreement may be waived other than by an
instrument in writing signed by the party against whom enforcement is sought.
"Required Holders" means (i) prior to the closing date of the Pre-Merger
Financing, the Investors entitled to purchase at the closing a majority of the
aggregate amount of Initial Common Shares issuable under the Securities Purchase
Agreement and the aggregate amount of shares issuable under the Investor
Warrants (without regard to any restriction or limitation on the exercise of the
Investor Warrant contained therein) and shall include the Lead Investor (as
defined in the Securities Purchase Agreement) and (ii) on or after the closing
of the Pre-Merger Financing, holders of at least a majority of the aggregate
amount of Purchased Securities issued and issuable under the Securities Purchase
Agreement and under the Investor Warrants (without regard to any restriction or
limitation on the exercise of the Investor Warrants or the delivery of the
Converted Additional Shares contained therein) held by the Investors or their
successors and assigns as of the applicable time of determination and shall
include the Lead Investor so long as the Lead Investor or any of its affiliates
holds any Purchased Securities.

Upon written notice by the non-breaching party, the Securities Purchase Agreement may be terminated and the sale and purchase of the Purchased Securities abandoned if the closing of the Pre-Merger Financing has not occurred on or before November 14, 2020, due to any party's failure to satisfy the conditions to closing. The Securities Purchase Agreement will terminate automatically upon any termination of the Merger Agreement.

Series A Warrants



The Series A Warrants will be issued on the warrant closing date, will have an
initial exercise price per share equal to 120% of per share Final Purchase
Price, will be immediately exercisable and will have a term of five years from
the date of issuance. The Series A Warrants issued to each Investor will
initially be exercisable for an amount of our common stock equal to the sum of
(i) the number of Converted Initial Shares issued to the Investor, (ii) the
number of Converted Additional Shares delivered or deliverable to the Investor
as of the warrant closing date and (iii) the number of shares, if any,
underlying the Series B Warrants held by the Investor as of the warrant closing
date.

The Series A Warrants will provide that, until the second anniversary of the
date on which the all shares of our common stock issued and issuable to the
Investors (including any shares underlying the Investor Warrants) (the
"Underlying Securities") may be sold without restriction or limitation pursuant
to Rule 144 (provided that we are current in our SEC filings, and if not, the
second anniversary of such later date on which the Public Information Failure is
cured and no longer prevents the Investors from selling all of the Underlying
Securities), if we publicly announce, issue or sell, enter into a definitive,
binding agreement pursuant to which we are required to issue or sell or are
deemed, pursuant to the provisions of the Series A Warrants, to have issued or
sold, any shares of our common stock for a price per share lower than the
exercise price then in effect, subject to certain limited exceptions, then the
exercise price of the Series A Warrants shall be reduced to such lower price per
share. Further, every ninth trading day up to and including the 45th trading day
(each, a "Reset Date"), the Series A Warrants will be adjusted downward (but not
increased) such that the exercise price thereof becomes 120% of the Reset Price
(as defined below), and the number of shares underlying the Series A Warrants
will be increased (but not decreased) to the quotient of (a) (i) the exercise
price in effect prior to such Reset (as defined below) multiplied by (ii) the
number of shares underlying the Series A Warrants prior to the Reset divided by
(b) the resulting exercise price. In addition, the exercise price and the number
of shares of our common stock issuable upon exercise of the Series A Warrants
will also be subject to adjustment in the event of any stock splits, dividends
or distributions or other similar transactions.

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Pursuant to the Series A Warrants, we will agree not to enter into, allow or be
party to certain fundamental transactions, generally including any merger with
or into another entity, sale of all or substantially all of our assets, tender
offer or exchange offer, or reclassification of our common stock (a "Fundamental
Transaction") until the 45th trading day immediately following the earlier to
occur of (x) such time as all of the Underlying Securities may be sold without
restriction or limitation pursuant to Rule 144 and without the requirement to be
in compliance with Rule 144(c)(1), and (y) one year after the warrant closing
date (the "Reservation Date"). Thereafter, upon any exercise of a Series A
Warrant, the holder shall have the right to receive, for each warrant share that
would have been issuable upon such exercise immediately prior to the occurrence
of a Fundamental Transaction, at the option of the holder (without regard to any
limitation on the exercise of the Series A Warrant), the number of shares of
common stock of the successor or acquiring corporation or of us, if we are the
surviving corporation, and any additional consideration (the "Alternate
Consideration") receivable as a result of such Fundamental Transaction by a
holder of the number of shares of our common stock for which the Series A
Warrant is exercisable immediately prior to such Fundamental Transaction
(without regard to any limitation on the exercise of the Series A Warrant).
Additionally, at the request of a holder delivered before the 90th day after the
consummation of a Fundamental Transaction, we or the surviving entity must
purchase such holder's warrant for the value calculated using the Black-Scholes
option pricing model as of the day immediately following the public announcement
of the applicable contemplated Fundamental Transaction, or, if such Fundamental
Transaction is not publicly announced, the date the Fundamental Transaction is
consummated.

The Series A Warrants will also contain a "cashless exercise" feature that
allows the holders to exercise the Series A Warrants without making a cash
payment. The Series A Warrants will be subject to a blocker provision which
restricts the exercise of the Series A Warrants if, as a result of such
exercise, the holder, together with its affiliates and any other person whose
beneficial ownership of our common stock would be aggregated with the holder's
for purposes of Section 13(d) of the Exchange Act would beneficially own in
excess of 4.99% or 9.99% of our outstanding common stock (including the shares
of our common stock issuable upon such exercise).

If we fail to issue to a holder of Series A Warrants the number of shares of our
common stock to which such holder is entitled upon such holder's exercise of the
Series A Warrants, then we shall be obligated to pay the holder on each day
while such failure is continuing an amount equal to 1.5% of the market value of
the undelivered shares determined using a trading price of our common stock
selected by the holder while the failure is continuing and if the holder
purchases shares of our common stock in connection with such failure ("Series A
Buy-In Shares"), then we must, at the holder's discretion, reimburse the holder
for the cost of such Series A Buy-In Shares or deliver the owed shares and
reimburse the holder for the difference between the price such holder paid for
the Series A Buy-In Shares and the market price of such shares, measured at any
time of the holder's choosing while the delivery failure was continuing.

Further, the Series A Warrants will provide that, in the event that we do not
have sufficient authorized shares to deliver in satisfaction of an exercise of a
Series A Warrant, then unless the holder elects to void such attempted exercise,
the holder may require us to pay an amount equal to the product of (i) the
number of shares that we are unable to deliver and (ii) the highest
volume-weighted average price of a share of our common stock as quoted on Nasdaq
during the period beginning on the date of such attempted exercise and ending on
the date that we make the applicable payment.

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Series B Warrants

The Series B Warrants will be issued to each Investor on the warrant closing
date, and each Investor's Series B Warrants will have an exercise price per
share of $0.0001, will be immediately exercisable and will expire on the day
following the later to occur of (i) the Reservation Date, and (ii) the date on
which the Investor's Series B Warrants have been exercised in full (without
giving effect to any limitation on exercise contained therein) and no shares
remain issuable thereunder. Each Investor's Series B Warrants will be initially
exercisable for an amount of our common stock equal to the number (if positive)
obtained by subtracting (i) the sum of (a) the number of Converted Initial
Shares issued to the Investor and (b) the number of Converted Additional Shares
delivered or deliverable to the Investor as of the warrant closing date, from
(ii) the quotient determined by dividing (a) the pro rata portion of the
Purchase Price paid by the Investor by (b) 85% of the average of the five lowest
volume-weighted average trading prices of a share of our common stock on Nasdaq
during the first ten trading days (or earlier at the election of any Investor)
immediately following the Closing, subject to the Floor Price.

Additionally, every Reset Date following (i) the earlier date to occur of (x)
such time as all of the Underlying Securities may be sold without restriction or
limitation pursuant to Rule 144 and (y) six months following the issuance date
(such earlier date, the "Six Month Reset Date") and (ii) if a Public Information
Failure has occurred at any time following the Six Month Reset Date, the earlier
to occur of (x) the date that such Public Information Failure is cured and no
longer prevents the holder from selling all of the Underlying Securities
pursuant to Rule 144 without restriction or limitation and (y) the earlier to
occur of (I) the date all of the Underlying Securities may be sold without
restriction or limitation pursuant to Rule 144 and without the requirement to be
in compliance with Rule 144(c)(1) and (II) one year after the issuance date
(each such date provided in the foregoing clauses (i), (ii) and (iii), an "End
Reset Measuring Date") (such 45 trading day period, the "Reset Period" and each
such 45th trading day after an End Reset Measuring Date, an "End Reset Date"),
the number of shares issuable upon exercise of each Investor's Series B Warrants
shall be increased ("Reset") to the number (if positive) obtained by subtracting
(i) the sum of (a) the number of Converted Initial Shares issued to the Investor
and (b) the number of Converted Additional Shares delivered or deliverable to
the Investor as of the warrant closing date, from (ii) the quotient determined
by dividing (a) the pro rata portion of the Purchase Price paid by the Investor,
by (b) the greater of (x) the arithmetic average of the five lowest dollar
volume-weighted average prices of a share of Rexahn Common Stock on Nasdaq
during the applicable Reset Period immediately preceding the applicable Reset
Date to date and (y) a floor price per share (the "Floor Price") calculated
based on a pre-money valuation (of the combined company, assuming for this
purpose the pre-money issuance of the Converted Initial Shares and Converted
Additional Shares) of $10 million (such number resulting in this clause (b), the
"Reset Price").

Pursuant to the Series B Warrants, we will agree not to enter into, allow or be
party to a Fundamental Transaction until the Reservation Date. Thereafter, upon
any exercise of a Series B Warrant, the holder shall have the right to receive,
for each warrant share that would have been issuable upon such exercise
immediately prior to the occurrence of a Fundamental Transaction, at the option
of the holder (without regard to any limitation on the exercise of the Series B
Warrant), the number of shares of common stock of the successor or acquiring
corporation or of us, if we are the surviving corporation, and any Alternate
Consideration receivable as a result of such Fundamental Transaction by a holder
of the number of shares of our common stock for which the Series B Warrant is
exercisable immediately prior to such Fundamental Transaction (without regard to
any limitation on the exercise of the Series B Warrant).

The Series B Warrants will also contain a "cashless exercise" feature that
allows the holders to exercise the Series B Warrants without making a cash
payment. The Series B Warrants will be subject to a blocker provision which
restricts the exercise of the Series B Warrants if, as a result of such
exercise, the holder, together with its affiliates and any other person whose
beneficial ownership of our common stock would be aggregated with the holder's
for purposes of Section 13(d) of the Exchange Act would beneficially own in
excess of 4.99% or 9.99% of our outstanding common stock (including the shares
of our common stock issuable upon such exercise).

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If we fail to issue to a holder of Series B Warrants the number of shares of our
common stock to which such holder is entitled upon such holder's exercise of the
Series B Warrants, then we shall be obligated to pay the holder on each day
while such failure is continuing an amount equal to 1.5% of the market value of
the undelivered shares determined using a trading price of our common stock
selected by the holder while the failure is continuing and if the holder
purchases shares of our common stock in connection with such failure ("Series B
Buy-In Shares"), then we must, at the holder's discretion, reimburse the holder
for the cost of such Series B Buy-In Shares or deliver the owed shares and
reimburse the holder for the difference between the price such holder paid for
the Series B Buy-In Shares and the market price of such shares, measured at any
time of the holder's choosing while the delivery failure was continuing.

Further, the Series B Warrants will provide that, in the event that we do not
have sufficient authorized shares to deliver in satisfaction of an exercise of a
Series B Warrant, then unless the holder elects to void such attempted exercise,
the holder may require us to pay an amount equal to the product of (i) the
number of shares that we are unable to deliver and (ii) the highest
volume-weighted average price of a share of our common stock as quoted on Nasdaq
during the period beginning on the date of such attempted exercise and ending on
the date that we make the applicable payment.

Financing Lock-Up Agreements



In connection with the Pre-Merger Financing, we and Ocuphire will enter into
additional lock-up agreements (the "Financing Lock-Up Agreements") with each
officer, director or other person that will be subject to Section 16 of the
Exchange Act, with respect to us immediately following the Closing (the
"Financing Lock-Up Parties"), pursuant to which each of the Financing Lock-Up
Parties will agree that until the date that is 90 calendar days after the
earlier of (i) such time as all of the Underlying Securities may be sold without
restriction or limitation pursuant to Rule 144 and (ii) six months after the
closing of the Pre-Merger Financing (provided that, if there is a Public
Information Failure, such date shall be such later date on which the Public
Information Failure is cured and no longer prevents the Investors from selling
all of the Underlying Securities), subject to certain customary exceptions, such
Financing Lock-Up Party will not and will cause its affiliates not to (A) sell,
offer to sell, contract or agree to sell, hypothecate, pledge, grant any option
to purchase, make any short sale or otherwise dispose of or agree to dispose of,
directly or indirectly, any shares of our common stock or common stock
equivalents, or establish or increase a put equivalent position or liquidate or
decrease a call equivalent position within the meaning of Section 16 of the
Exchange Act with respect to any shares of Rexahn Common Stock or common stock
equivalents owned directly by the Financing Lock-Up Parties (including holding
as a custodian) or with respect to which the undersigned has beneficial
ownership within the rules and regulations of the SEC (collectively, the
"Subject Shares"), or (B) enter into any swap or other arrangement that
transfers to another, in whole or in part, any of the economic consequences of
ownership of any of the Subject Shares, whether any such transaction described
in clause (A) or (B) above is to be settled by delivery of shares of our common
stock or other securities, in cash or otherwise, (C) make any demand for or
exercise any right or cause to be filed a registration statement, including any
amendments thereto, with respect to the registration of any shares of our common
stock or common stock equivalents or (D) publicly disclose the intention to do
any of the foregoing.

Leak-Out Agreements

In connection with the Pre-Merger Financing, each Investor will enter into a
leak-out agreement with us limiting its daily sales to no more than its pro rata
portion, based on such Investor's investment amount, of 30% of the daily traded
volume as reported by Bloomberg, L.P.

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COVID-19

The outbreak of the COVID-19 disease, which the World Health Organization
declared a pandemic in March 2020, has led to disruption in the global economy
and the biopharmaceutical industry. The extent of the COVID-19 pandemic's impact
on our business, financial condition and results of operations, as well as on
our ability to consummate the Merger, is highly uncertain and will depend on
various factors, including the duration and scope of the pandemic, restrictions
on business and social distancing guidelines that may be requested or mandated
by governmental authorities, other actions taken to contain the impact of the
pandemic, and our access to additional capital.

Results of Operations

Comparison of the Three and Six Months Ended June 30, 2020 and June 30, 2019

Total Revenues



We had no revenues for the three months ended June 30, 2020 and 2019.  We
recorded revenues of $1,150,000 during the six months ended June 30, 2020,
consisting of $250,000 earned from the HaiChang License Agreement and $900,000
from the BioSense License and Assignment Agreement.  We had no revenues for the
six months ended June 30, 2019.

General and Administrative Expenses



General and administrative expenses consist primarily of salaries and related
expenses for executive, finance and other administrative personnel, recruitment
expenses, professional fees, and other corporate expenses, including business
development, investor relations, and general legal activities.

General and administrative expenses increased approximately $777,000, or 58.0%
to approximately $2,117,000 for the three months ended June 30, 2020 compared to
approximately  $1,340,000 for the three months ended June 30, 2019.  General and
administrative expenses increased approximately $337,000, or 11.1% to
approximately $3,373,000 for the six months ended June 30, 2020 compared to
approximately $3,036,000, for the six months ended June 30, 2019. The increases
were primarily attributable to increased legal and professional fees related to
the Merger Agreement, offset by decreases in personnel and operating costs
resulting from the streamlining of operations.

Research and Development Expenses



Research and development costs are expensed as incurred.  These costs consist
primarily of salaries and related personnel costs, and amounts paid to contract
research organizations, hospitals and laboratories for the provision of services
and materials for drug development and clinical trials.  Our research and
development expenses are currently related to our oncology drug candidates.

Research and development expenses decreased approximately $1,416,000, or 85.9%,
to approximately $232,000 for the three months ended June 30, 2020, from
approximately $1,648,000 for the three months ended June 30, 2019. Research and
development expenses decreased approximately $3,203,000, or 82.3%, to
approximately $688,000 for the six months ended June 30, 2020, from
approximately $3,891,000 for the six months ended June 30, 2019.  The decreases
are a result of the completion of our RX-3117 and RX-5902 clinical trials, and
decreased drug manufacturing costs.

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The table below summarizes the approximate amounts incurred in each of our
research and development projects for the three and six months ended June 30,
2020 and 2019:

                                             For the Three Months Ended          For the Six Months Ended
                                                      June 30,                           June 30,
                                               2020               2019             2020             2019
Clinical Candidates:
RX-3117                                    $      86,000       $ 1,058,000     $    412,900      $ 2,136,400
RX-5902                                            7,500           187,800           11,700          530,200
RX-0201                                                -            55,300            1,800          171,100

Preclinical, Personnel and Overhead              138,107           347,301  

261,997 1,052,931

Total Research and Development Expenses $ 231,607 $ 1,648,401

$ 688,397 $ 3,890,631

We expect total research and development expenses to decrease in the remainder of 2020 as compared to the three and six months ended June 30, 2020 as we complete our Phase 2a clinical trial of RX-3117 with Abraxane and progress toward consummation of the Merger.

Interest Income

Interest income decreased approximately $91,000 and $138,000, or 93.7% and 77.3%, respectively, for the three and six months ended June 30, 2020, respectively, compared to the same periods in 2019. The decreases were primarily attributable to lower interest rates and balances of cash, cash equivalents and marketable securities for the three and six months ended June 30, 2020 compared to the same periods in 2019.

Unrealized (Loss) Gain on Fair Value of Warrants



Our liability-classified warrants are recorded at fair value, and the warrants
are valued using a lattice model.  Changes in the fair value of warrants are
recorded as an unrealized gain or loss in our statement of operations.  During
the three months ended June 30, 2020 and 2019, we recorded unrealized (losses)
gains on the fair value of our warrants of approximately $(169,000) and
$427,000, respectively.  During the six months ended June 30, 2020 and 2019, we
recorded unrealized (losses) gains on the fair value of our warrants of
approximately $(227,000) and $1,941,000, respectively.  Estimating fair values
of warrants requires the development of significant and subjective estimates
that may, and are likely to, change over the duration of the warrants due to
related changes to external market factors.  The large unrealized gain for the
three and six months ended June 30, 2019 primarily resulted from a significant
decrease in the stock price of the underlying common stock at the end of this
period compared to the beginnings of this period.

Net Loss



As a result of the above, net loss for the three and six months ended June 30,
2020 was approximately $2,511,000 and $3,098,000, or $0.62 and $0.77 per share,
respectively, compared to approximately $2,464,000, and $4,807,000, or $0.61 and
$1.23 per share, respectively, for the three and six months ended June 30, 2019.

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Liquidity and Capital Resources

Current and Future Financing Needs



We have incurred negative cash flow from operations since we started our
business.  We expect to continue to incur negative cash flow and operating
losses.  We have spent, and if the Merger is not consummated, expect to continue
to spend, substantial amounts in connection with implementing our business
strategy, including our planned product development efforts, clinical trials and
research and development efforts  We believe that our cash and cash equivalents
of approximately $9.2 million as of June 30, 2020 will be sufficient to cover
our cash flow requirements for our current activities for at least the next 12
months following the issuance of the financial statements contained in this
Quarterly Report, assuming the Merger does not close.  If for any reason the
Merger does not close, we would need to raise additional capital to continue to
fund the further development of product candidates and our operations
thereafter. If we are unable to maintain sufficient financial resources, our
business, financial condition and results of operations will be materially and
adversely affected. This could affect future development and business
activities, such as future clinical studies and/or other future ventures. There
can be no assurance that we will be able to obtain the needed financing on
acceptable terms or at all. Additionally, equity or debt financings may have a
dilutive effect on the holdings of our existing stockholders.

Cash Flows



Cash used in operating activities was approximately $3,011,000 for the six
months ended June 30, 2020.  The operating cash flows during the six months
ended June 30, 2020 reflect a net loss of approximately $3,098,000, a net
increase of cash components of working capital and non-cash charges totaling
$87,000. Cash used in operating activities was approximately $6,187,000 for the
six months ended June 30, 2019.  The operating cash flows during the six months
ended June 30, 2019 reflect a net loss of approximately $4,807,000, an
unrealized gain on the fair value of warrants of approximately $1,941,000, and a
net increase of cash components of working capital and non-cash charges totaling
approximately $561,000.

Cash provided by investing activities was $3,000,000 from the redemption of
marketable securities for the six months ended June 30, 2020.  Cash used in
investing activities was approximately $2,901,000 for the six months ended June
30, 2019 which consisted of approximately $8,888,000 and approximately $19,000
from the purchases of marketable securities and equipment, respectively, offset
by approximately $6,000 from the sale of equipment and $6,000,000 from the
redemption of marketable securities.

There was no cash provided by financing activities for the six months ended June
30, 2020.  Cash provided by financing activities was approximately $7,654,000
for the six months ended June 30, 2019, which consisted of net proceeds from our
underwritten offering in January 2019.

Contractual Obligations



We have a variety of contractual obligations, as more fully described in the
2019 Form 10-K.  These obligations include, but are not limited to, contractual
obligations in connection with license agreements (including related milestone
payments), lease payments, employee compensation and incentive program expenses,
and contracts with various vendors for services.  As of June 30, 2020, the total
estimated cost to complete our contracts with vendors for research and
development services was approximately $210,000 under the terms of the
applicable agreements.  All of these agreements may be terminated by either
party upon appropriate notice as stipulated in the respective agreements.

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