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News about Protagonist Therapeutics, Inc. (NASDAQ: PTGX) centers on its progress as a discovery-through-late-stage development biopharmaceutical company advancing peptide-based drug candidates. Company announcements frequently highlight clinical and regulatory milestones for its lead investigational therapies, icotrokinra and rusfertide, as well as updates from its broader pipeline and collaborations.
Investors following PTGX news will see regular coverage of icotrokinra, a first-in-class investigational targeted oral peptide that selectively blocks the IL-23 receptor. Press releases describe data from Phase 3 ICONIC studies in moderate-to-severe plaque psoriasis, including ICONIC-LEAD, ICONIC-TOTAL, and ICONIC-ADVANCE 1 and 2, as well as the Phase 2b ANTHEM-UC trial in ulcerative colitis. News items also report on regulatory submissions, such as the New Drug Application to the U.S. FDA and an application to the European Medicines Agency for plaque psoriasis.
Coverage of rusfertide focuses on its development for polycythemia vera in collaboration with Takeda. News releases describe Phase 3 VERIFY study results, long-term extension data from THRIVE, and the submission of a New Drug Application to the FDA for adults with polycythemia vera. These updates often include details on hematocrit control, phlebotomy requirements, patient-reported outcomes, and regulatory designations such as Breakthrough Therapy, Orphan Drug, and Fast Track status.
Additional PTGX news includes presentations at major medical and scientific conferences, such as the American Society of Hematology Annual Meeting, European Academy of Dermatology and Venereology Congress, American College of Gastroenterology meeting, and the J.P. Morgan Healthcare Conference. The company also issues periodic financial result and corporate update releases, which summarize recent clinical achievements, collaboration developments with Johnson & Johnson and Takeda, and progress in earlier-stage programs like PN-881, PN-477, and the oral hepcidin initiative.
For readers tracking PTGX, this news stream provides insight into Protagonist’s clinical data, regulatory interactions, partnership activities, and pipeline evolution as described in its own public communications.
Protagonist Therapeutics (Nasdaq:PTGX) announced on September 15, 2020, the issuance of an inducement award to Matthew Gosling, the newly appointed Executive Vice President and General Counsel. This award includes an option to purchase 100,000 shares of common stock at an exercise price of $21.66, matching the stock's closing price on the grant date. The shares will vest over four years, with the first 25% vesting after one year. The award is part of Mr. Gosling's employment terms approved by the company's compensation committee.
Protagonist Therapeutics (NASDAQ: PTGX) has announced that its CEO, Dinesh V. Patel, Ph.D., will engage in a fireside chat at the H.C. Wainwright 22nd Annual Global Investment Conference on September 14, 2020, at 11 a.m. EDT. The event will be available via live and archived webcast on the company's investor website. Protagonist Therapeutics focuses on developing novel peptide-based therapeutics, with three clinical-stage assets: PTG-300 for blood disorders, PTG-200 for inflammatory bowel disease, and PN-943 also targeting inflammatory bowel disease.
Protagonist Therapeutics (NASDAQ:PTGX) will host a webinar on Sept. 11, 2020, from 12 p.m. to 1:30 p.m. EDT, titled "PTG-300 Opportunity Update". The event will discuss clinical needs in polycythemia vera and market research for PTG-300, an injectable hepcidin mimetic aimed at treating blood disorders. Presenters include Dr. Ronald Hoffman from the Icahn School of Medicine and Dr. Srdan Verstovsek from MD Anderson Cancer Center. The webinar will be accessible online and archived afterward for future viewing.
Protagonist Therapeutics (Nasdaq:PTGX) has appointed Sarah O'Dowd as an independent director on its Board, enhancing its governance with her extensive experience in the biopharmaceutical sector. O'Dowd's previous roles include key positions at Lam Research and FibroGen. She replaces Chaitan Khosla, who is stepping down. CEO Dinesh V. Patel emphasized her strategic expertise as vital for Protagonist's growth, particularly with its clinical assets focused on hematology/oncology and inflammatory bowel diseases. O'Dowd expressed eagerness to contribute to Protagonist's vision during this growth phase.
Protagonist Therapeutics (PTGX) reported its Q2 2020 financial results, highlighting significant advancements in its clinical programs. The company moved three candidates into Phase 2 trials, including PTG-300 for polycythemia vera and two oral candidates for inflammatory bowel disease. Financially, PTGX raised $122 million through a secondary offering and has sufficient resources to fund operations through mid-2023. The net loss for Q2 was $19.4 million, improving from $29.2 million the previous year. Revenue from collaborations rose to $6.2 million this quarter, compared to a loss in revenue last year.
On June 17, 2020, Protagonist Therapeutics (Nasdaq: PTGX) announced that the FDA granted Orphan Drug Designation for PTG-300, a synthetic peptide mimetic for treating polycythemia vera (PV). This milestone highlights PTG-300's potential to address patient needs in PV treatment. The Phase 2 results showed a robust clinical response with effective hematocrit control. The FDA’s designation provides benefits like marketing exclusivity and tax credits, vital for developing treatments for rare diseases affecting under 200,000 patients in the U.S.
Protagonist Therapeutics, Inc. (NASDAQ:PTGX) announced that Dinesh V. Patel, Ph.D., President and CEO, will participate in a fireside chat at the BMO Prescriptions for Success Healthcare Conference on June 23, 2020, at 1:00 p.m. EDT. The event will be accessible via a live and archived webcast on the company’s Investors section of its website. Protagonist is known for its proprietary technology platform aimed at developing novel peptide-based therapeutics, including three clinical-stage assets like PTG-300 and PTG-200.