Annovis Bio completes enrollment in Phase 3 buntanetap trial for early Alzheimer's
The 850-patient study exceeded its original enrollment target, with symptomatic data expected in Q1 2027 and disease-modifying data in Q1 2028.
SEC filing
The 850-patient study exceeded its original enrollment target, with symptomatic data expected in Q1 2027 and disease-modifying data in Q1 2028.
SEC filing
The new drug application for an intravenous sodium bicarbonate solution received original approval as a Type 5 new formulation or new manufacturer submission.
Drugs@FDA
The agency cleared BLA761445 for isatuximab-irfc under the brand name Sarclisa Escena, with an original approval dated July 9, 2026.
Drugs@FDA
The trial in transthyretin-mediated amyloid cardiomyopathy did not show a statistically significant benefit over placebo, though a monotherapy subgroup showed a nominally significant effect.
SEC filing
The company swapped remaining legacy EIB warrants for a simplified instrument, part of a broader refinancing tied to lanifibranor's MASH program.
SEC filing
The CARDIO-TTRansform study failed to show a statistically significant benefit over placebo, though a monotherapy subgroup showed a nominally significant result.
SEC filing
The license grants rights to a patented technology and know-how for use in aerospace and defense applications, with royalties and milestone obligations attached.
SEC filing (2)
All active patients in both Part 3 cohorts reached their highest target doses, with topline data still expected in the fourth quarter of 2026.
SEC filing
Biohaven's chief scientific officer moves to a new part-time innovation role while David Pirman takes over discovery operations, effective July 13, 2026.
SEC filing
William Turner steps down from the CRO role and moves to a special advisor position, with Nancy Bowman set to replace him.
SEC filing
Kyverna will pay a $187,500 fee to extend its remaining Term A loan draw window to the end of 2026, with further changes tied to full drawdown.
SEC filing
At its July 8, 2026 annual meeting, Traws Pharma stockholders approved a 2,000,000-share increase to the company's incentive compensation plan and elected seven directors.
SEC filing
The Houston biotech named Kathleen Rubins, Ph.D. a Class III director effective July 8, 2026, following Matt Link's resignation from the board.
SEC filing
Roche deal brings $700 million upfront and expands the drug into CSU and MS as Nurix advances its CLL pivotal trials.
SEC filing
The animal health company posted preliminary second-quarter sales of $7.2 million, with domestic growth offsetting a decline in international sales.
SEC filing
Sandra Calvin plans to step down as CAO and PAO after filing the 2027 annual report, with John Torell expected to take.
SEC filing
The spine biologics company sold shares and warrants to a single institutional investor, with potential added proceeds of up to $6 million if warrants are exercised.
SEC filing
The Novato, California biotech reported selling half of a planned $20 million offering to two investors as of a Form D filed with the SEC.
SEC filing
The deal brings Tarsus a Phase 2b/3-tested ocular antiseptic aimed at reducing pain and corneal damage from intravitreal injections, with a Phase 3 study planned to start enrolling in the first half of 2027.
SEC filing
The FDA meeting outcome supports a single-dose trial design and a possible single-trial path to registration for the neuropathic corneal pain candidate.
SEC filing
The combined company, to be named Scipher Medicine, plans a Phase 2 trial of nebokitug in rheumatoid arthritis guided by an AI patient-selection platform, with a readout expected in H1 2028.
SEC filing
Moderna appointed Michael McDonnell to its Board of Directors and Audit Committee, effective July 8, 2026, as the company prepares for potential product launches.
SEC filing
Evolus will handle U.S. development and regulatory work for the European skin-boosting injectable, with no upfront payment to IBSA.
SEC filing
GSK's termination follows failed trials for both progranulin-elevating antibodies developed under the partnership, and Alector separately paid off its outstanding loan.
SEC filing
The Zurich-based cell therapy company said the move follows a successful FDA Type B Pre-IND meeting for its lead program, NCEL-101.
SEC filing
The Hudson, Massachusetts-based company reported five investors in a securities sale that began July 6, 2026, with no sales commissions paid.
SEC filing
The clinical-stage oncology company added Bender, former Day One Biopharmaceuticals CEO, as it advances its lead candidate bel-sar toward potential approval.
SEC filing
The meeting, adjourned in June for lack of quorum, reconvened on July 8, 2026 with stockholders backing three director nominees and a 900,000-share increase to the 2025 incentive plan.
SEC filing
Ovid's board appointed Carter to succeed Rona effective July 6, 2026, following what the company said was a mutual decision on Rona's exit.
SEC filing
Ferrante notified the board of her departure on July 1, 2026, with the company saying the move was unrelated to any dispute over its operations.
SEC filing
The companies ended their September 2025 agreement on July 6, 2026, after Amneal declined to order product under the arrangement.
SEC filing
The FDA cleared an efficacy-related supplement for the mometasone furoate and olopatadine hydrochloride combination spray on July 7, 2026.
Drugs@FDA
Tvardi Therapeutics reported that TTI-109 matched TTI-101's exposure with better tolerability, supporting plans to advance into Phase 2 pending funding.
SEC filing
Bora paid $122.5 million for MacroGenics' Rockville facility and related assets, hiring about 140 former staff and taking over CDMO operations effective June 30, 2026.
SEC filing
The company sold shares, pre-funded warrants and common warrants at $0.7101 combined, with Maxim Group as placement agent and net proceeds of about $3.335 million.
SEC filing
Lifeward Ltd. restructured its senior secured convertible notes with Oramed Pharmaceuticals and closed an initial tranche of new notes on July 6, 2026, with a matching second tranche contingent on sales or share price.
SEC filing
The company borrowed an additional $1.9 million on June 30, 2026 under its revolving credit facility with Parkview Holdings One LLC, an 8-K filing shows.
SEC filing
FDA’s official End-of-Phase 2 minutes confirm a single pivotal trial plus confirmatory data could support approval, with Phase 3 targeted to start by year-end 2026.
SEC filing
The board installed President Donn Casale as CEO effective immediately, ousting Richard Lowenthal without cause.
SEC filing
Andrew Levin left the Vor Biopharma board effective immediately, and David Zaccardelli was named to fill the seat starting July 7, 2026.
SEC filing
Fred Middleton plans to retire from the board at the company's 2026 annual meeting, which will return the board to seven members.
SEC filing