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Hilary Swank ‘Took the Time to Learn’ About Make-A-Wish Mom’s Terminally Ill Kids After Altercation
The mother of two terminally ill boys has opened up about making peace with Oscar winner Hilary Swank following an alleged ...
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Hilary Swank apologizes for lashing out at mom taking terminally ill sons on Make-A-Wish trip
Swank allegedly accused a mom taking her two terminally ill sons on a trip to Disneyland of snapping her picture at the ...
The Muscular Dystrophy Association (MDA) today announced more than $2.7 million in new research grants to advance groundbreaking discoveries across multiple neuromuscular diseases, including ...
Capricor Therapeutics said Wednesday that its cell therapy significantly improved muscle and heart function in patients with ...
Nine years after Sarepta Therapeutics’ Exondys 51 won a controversial FDA approval to treat a subset of patients with Duchenne muscular dystrophy, challenger from Massachusetts biotech Dyne ...
Atossa Therapeutics, Inc. (Nasdaq: ATOS) ("Atossa" or the "Company"), a clinical-stage biopharmaceutical company developing novel therapies in oncology and other areas of high unmet clinical need, ...
Dyne Therapeutics plans to submit its next-gen Duchenne muscular dystrophy drug to the FDA after a successful trial.
Atossa Therapeutics, Inc. (NASDAQ: ATOS) stock is trading higher on Thursday. Here's what investors need to know.
Investor's Business Daily on MSN
Capricor skyrockets 535% after getting vindication in muscular dystrophy
Capricor stock skyrocketed to an eight-year high Wednesday, catapulting more than 300%, on positive results for its Duchenne ...
Ractigen Therapeutics, a pioneering developer of small activating RNA (saRNA) therapeutics, today announced the successful dosing of the first patient in its investigator-initiated ...
Jada Bafus told Page Six that she and the actress quickly came to realize it was a case of “two triggered mothers” having a ...
Ractigen Therapeutics, a pioneering developer of small activating RNA (saRNA) therapeutics, today announced the successful dosing of the first patient in its investigator-initiated trial (IIT) of ...
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