Sotatercept safe and effective against pulmonary arterial hypertension: Phase 3 STELLAR trial

Written By :  Dr. Kamal Kant Kohli
Published On 2022-10-11 14:00 GMT   |   Update On 2022-10-11 17:24 GMT

USA: Patients with pulmonary arterial hypertension (PAH) who received sotatercept showed a statistically significant and clinically meaningful improvement in 6-minute walk distance (6MWD) from baseline at 24 weeks, according to top-line results from the Phase 3 STELLAR trial. The positive top-line results from the pivotal Phase 3 STELLAR trial were announced by Merck.The trial evaluated...

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USA: Patients with pulmonary arterial hypertension (PAH) who received sotatercept showed a statistically significant and clinically meaningful improvement in 6-minute walk distance (6MWD) from baseline at 24 weeks, according to top-line results from the Phase 3 STELLAR trial.

The positive top-line results from the pivotal Phase 3 STELLAR trial were announced by Merck.The trial evaluated the safety and efficacy of sotatercept, an investigational activin receptor type IIA-Fc (ActRIIA-Fc) fusion protein being evaluated as an add-on to stable background therapy for the treatment of pulmonary arterial hypertension (PAH) (WHO Group 1).

The trial met its primary efficacy outcome measure, demonstrating a statistically significant and clinically meaningful improvement in 6-minute walk distance (6MWD, which measures how far patients can walk in 6 minutes) from baseline at 24 weeks. Eight of nine secondary efficacy outcome measures achieved statistical significance, including the outcome measure of the proportion of participants achieving multi-component improvement (defined as improvement in 6MWD, improvement in N-terminal pro-B-type natriuretic peptide (NT-proBNP) level, and either improvement in WHO FC or maintenance of WHO FC II), and the outcome measure of time to death or the first occurrence of a clinical worsening event (TTCW).

The Cognitive/Emotional Impacts domain score of PAH-SYMPACT, which was assessed as the ninth and final secondary outcome measure, did not achieve statistical significance. The overall safety profile of sotatercept in STELLAR was in general consistent with what has been observed in Phase 2. Results from the study will be presented at an upcoming scientific congress.

The results from the secondary efficacy outcomes, including a favorable benefit seen in patients' time to a clinical-worsening event, are especially noteworthy," said Dr. Dean Y. Li, president, Merck Research Laboratories. "We believe that in totality, the results observed in the STELLAR study suggest that sotatercept has the potential to transform the treatment of patients with PAH. We are moving with urgency on our regulatory applications to bring this investigational therapy to these patients."

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