Medifirst Solutions Inc. announced that they are working with its affiliate and consulting groups in setting up a clinical trial for the treatment in reducing Oral Mucositis that will include three testing locations. Medifirst recently announced a new expansion and direction for its Time Machine Therapeutic Laser for the application of Photobiomodulation (PBM) to treat a side effect of cancer therapy called Oral Mucositis. This would involve adding a new claim and a new name for the laser treatment program via an FDA pre-submission application for the FDA 510(k) cleared Time Machine TTML-8102000 Laser Thermal Therapeutic Device. Discussions are underway with two Universities that have expressed interest to participate. Additionally, Dr. Ronald L. Rubin DMD, an Oral & Maxillofacial Surgeon and the Medifirst Medical Director, will conduct one of the studies in his Florida practice. Dr. Rubin, a Specialist in Head and Neck Cancer, (he was granted an American Cancer Society Fellowship in Head and Neck Cancer at the Tufts-New England Medical Center in Boston) will be setting up an IRB for the treatment protocols and is the Chief Clinical Investigator that will guide the Universities with the treatment protocols and over-seeing the clinical review. It must be noted that the Company cannot guarantee the participation of the Universities until all the details and procedures have been formulated and all terms agreed to. CPT Code: It is the opinion of the Company that Photobiomodulation is becoming a mainstream treatment modality in the medical community and the FDA 510(k) cleared TTML-810/2000 Infrared laser has shown that its safety and efficiency to meet the proper guideline for a CPT approval process. Although they cannot guarantee a new code will be approved, they believe that the Time Machine TTML-810/2000 Infrared Laser, in the coming months, may receive a CPT code for specific pain treatments. CPT codes are the billing codes used for reimbursement for services and treatments by the healthcare providers. Home Study: A Medifirst affiliate partner has previously filed for a $3,000,000 grant to perform a study for home usage (OTC) for the Time Machine TTML-810/2000 Infrared Laser. The company received the first round of comments back from the NIH grant oversight committee and will be submitting its answers back for an October review meeting date. With millions of people suffering from everyday pain, Medifirst considers “home use” a major priority if the laser can be proven safe and FDA cleared for home use. Once approved, the patient would receive a prescription and pick up the laser at their doctor’s office or medical supply store. Since the process is ongoing, Medifirst cannot, at this time, guarantee the grant will be approved. Medifirst anticipates further updates and details regarding these developments in the upcoming weeks and months.