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Study Evaluating the Safety, Tolerability and Preliminary Pharmacokinetics and Pharmacodynamics of MYK-461

Completed · Phase 1 · NCT02329184

Conditions: Hypertrophic Cardiomyopathy

At a glance

Research payments reported, 2025
$915,244
U.S. investigators named
23
Sites paid
21
Planned or actual enrollment
15

About the trial

Sponsor
MyoKardia, Inc.
Tested
MYK-461 (drug)
Dates
Started 2014-12; completion 2016-04
Results posted
Not yet

The purpose of this study is to establish initial safety, tolerability, pharmacokinetics and pharmacodynamics of MYK-461 in human subjects. This is a sequential group, single ascending (oral) dose study in NYHA Class I, II, or III patient volunteers aged 18-65 years.

From ClinicalTrials.gov, last updated 2016-09-14. Full record, eligibility and contacts (opens in a new tab)

Industry funding

E.r. Squibb & Sons, L.l.c. reported $915,244 in research payments for this study in 2025 (22 payments).

Products named: Camzyos

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.