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Edgewise Therapeutics Advances EDG-7500 Study for Hypertrophic Cardiomyopathy

Edgewise Therapeutics Advances EDG-7500 Study for Hypertrophic Cardiomyopathy

Edgewise Therapeutics, Inc. ((EWTX)) announced an update on their ongoing clinical study.

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Edgewise Therapeutics, Inc. is conducting a study titled ‘An Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of EDG-7500 in Adults With Hypertrophic Cardiomyopathy.’ The study aims to assess the safety and effects of EDG-7500 in adults with hypertrophic cardiomyopathy, focusing on both obstructive and nonobstructive forms. This research is significant as it explores potential new treatments for this heart condition.

The intervention being tested is EDG-7500, a drug designed to be administered in both liquid suspension and solid oral formulations. The purpose is to evaluate its safety and effectiveness in treating hypertrophic cardiomyopathy.

The study is interventional, non-randomized, and follows a sequential intervention model without masking. Its primary purpose is treatment, focusing on the effects of EDG-7500 in different dosing regimens.

The study began on March 18, 2024, with the last update submitted on August 25, 2025. These dates are crucial as they indicate the study’s progress and the timeline for potential results.

This update could positively impact Edgewise Therapeutics’ stock performance by boosting investor confidence in their pipeline. The study’s progress might also influence the competitive landscape in the cardiomyopathy treatment market.

The study is currently ongoing, with further details available on the ClinicalTrials portal.

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