Larimar Therapeutics names John B. Harlow Jr. president and COO
The board's appointment, effective September 29, 2026, comes with a $560,000 base salary, a $35,000 signing bonus, and inducement equity grants.
SEC filing
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The board's appointment, effective September 29, 2026, comes with a $560,000 base salary, a $35,000 signing bonus, and inducement equity grants.
SEC filing
ADARx Pharmaceuticals sold 26.25 million shares in its Nasdaq debut and will use proceeds to fund late-stage siRNA programs including a Phase 3 hereditary angioedema trial.
SEC filing
Zhang, formerly Novartis International's Chief Commercial Officer, succeeds interim CEO Alan Bash, who returns to lead the CARVYKTI business.
SEC filing
The clinical-stage oncology company named the former Incyte executive as a Class III director effective September 9, 2026.
SEC filing
Novartis initiated a Phase 2a/b study of the VAV1-directed molecular glue degrader, triggering a $50 million milestone payment to Monte Rosa under their license agreement.
SEC filing
Lp(a)HORIZON did not reduce cardiovascular events despite lowering Lp(a) levels, Ionis and partner Novartis reported.
SEC filing
The San Diego siRNA drugmaker seeks to list its three clinical-stage and two preclinical programs, backed by a $335 million AbbVie upfront payment.
SEC filing
The appointment, effective immediately, comes ahead of the company's planned Phase 3 start for its lead osteoporosis candidate EB613.
SEC filing
The biopharmaceutical company named Blumenkranz a Class II director on August 10, 2026, while longtime director Satter resigned effective immediately before the appointment.
SEC filing
Phase 3 asthma trials expand recruitment and an oncology combination study completes enrollment as cash falls to $457.4 million.
SEC filing
Monte Rosa completed enrollment in its MRT-8102 cardiovascular study, activated two other Phase 2 trials, and said cash on hand should fund operations into 2029.
SEC filing
The efficacy supplement for the radioligand therapy Pluvicto was approved with a status date of July 31, 2026.
Drugs@FDA
Sephience sales drove product revenue growth as the company reported net income and advanced its Huntington's disease and Friedreich's ataxia programs.
SEC filing
The clinical-stage biotech brought on the former Ferring uro-oncology executive to help guide strategy for its bladder cancer therapy NDV-01.
SEC filing
Novartis received priority-review approval for a seventh supplement to Fabhalta's original new drug application, expanding the drug's approved use.
Drugs@FDA