Alnylam Pharmaceuticals, Inc.

News & Events zu Alnylam Pharmaceuticals, Inc. (ALNY)

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ALNY-News

ALNY-Events

9/29 09:30

Alnylam Launches AMVUTTRA Educational Initiative

Alnylam Pharmaceuticals announced the launch of AMVUTTRA 'Play by Play,' a U.S. educational initiative featuring former professional athletes living with the cardiomyopathy of transthyretin-mediated amyloidosis and the care teams who support them. Through personal stories and expert perspectives, 'Play by Play' aims to help people recognize the symptoms of ATTR-CM earlier and encourage informed conversations with healthcare professionals to help patients advocate for their diagnosis and treatment. 'Play by Play' kicks off with Pete Shaw, a former professional football player living with ATTR-CM, alongside his wife and caregiver, Kari, and one of his cardiologists, Rajeev Mohan, M.D. Together, they share Pete's journey from experiencing symptoms that were mistakenly attributed to football or aging, to pursuing testing, receiving an ATTR-CM diagnosis, and ultimately starting treatment with AMVUTTRA, a transthyretin silencer, as part of his game plan for ATTR-CM management.

8/30 16:30

Alnylam Presents RNAi Data for Cardiovascular Disease

Alnylam Pharmaceuticals announced new data at the European Society of Cardiology, ESC, Congress 2026 demonstrating the strength of RNAi-powered silencing for cardiovascular disease. The findings further reinforce the clinical profile of AMVUTTRA across transthyretin amyloidosis, ATTR, patient populations, treatment settings, and manifestations of disease. Additionally, the data expand the potential application of RNAi to uncontrolled hypertension, the world's leading cause of cardiovascular disease. "With the power of our RNAi therapeutics platform, we have the potential to make a transformational impact on cardiovascular care," said Pushkal Garg, M.D., Chief Research and Development Officer at Alnylam. "The data presented at ESC demonstrate the consistency of clinical outcomes achieved by RNAi-powered TTR silencing, reinforcing our conviction in AMVUTTRA as a first-line treatment option for ATTR-CM. With zilebesiran, we have the potential to extend the precision and durability of RNAi to uncontrolled hypertension. Together, these programs reflect our ambition to change the course of cardiovascular disease for patients with high unmet need."

8/28 09:00

AstraZeneca and Ionis Trial Fails to Meet Primary Efficacy Endpoint

The CARDIO-TTRansform trial investigating eplontersen in patients with transthyretin-mediated amyloid cardiomyopathy did not meet its primary efficacy endpoint, according to results presented at the European Society of Cardiology Congress. The primary endpoint was a composite of cardiovascular mortality and recurrent cardiovascular events. There were 381 primary endpoint events in 210 patients receiving eplontersen compared with 392 events in 231 patients receiving placebo. Eplontersen produced suppression of circulating serum TTR, consistent with the expected pharmacodynamic effect of TTR gene silencing, as assessed by a prespecified exploratory endpoint through Week 140. The trial was funded by AstraZeneca (AZN) and Ionis Pharmaceuticals (IONS). Shares of Ionis are down 2% to $61.43 in premarket trading. Alnylam (ALNY), which is also developing a treatment for transthyretin amyloidosis with cardiomyopathy, is down 5% to $224.01.

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