A Study to Evaluate the Efficacy, Safety, and Tolerability of MYK-224 in Participants With Symptomatic Obstructive Hypertrophic Cardiomyopathy

PHASE2TerminatedINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

January 18, 2023

Primary Completion Date

August 19, 2024

Study Completion Date

February 27, 2025

Conditions
Cardiomyopathy, Hypertrophic
Interventions
DRUG

MYK-224

Specified dose on specified days

Trial Locations (25)

15006

Local Institution - 0009, A Coruña

18014

Local Institution - 0022, Granada

20138

Local Institution - 0029, Milan

27710

Local Institution - 0013, Durham

28035

Local Institution - 0010, Majadahonda

29010

Local Institution - 0008, Málaga

30120

Local Institution - 0002, El Palmar

40138

Local Institution - 0027, Bologna

45267

Local Institution - 0031, Cincinnati

46026

Local Institution - 0003, Valencia

50134

Local Institution - 0005, Florence

84132

Local Institution - 0006, Salt Lake City

90048

Local Institution - 0014, Los Angeles

92037

Local Institution - 0026, La Jolla

94158-2156

Local Institution - 0016, San Francisco

66103-2937

Local Institution - 0001, Kansas City

10032-3802

Local Institution - 0032, New York

44195-0001

Local Institution - 0015, Cleveland

97239-3011

Local Institution - 0024, Portland

37205-2202

Local Institution - 0021, Nashville

78229-3900

Local Institution - 0025, San Antonio

40-555

Local Institution - 0011, Katowice

54-049

Local Institution - 0030, Wroclaw

03010

Local Institution - 0028, Alicante

08036

Local Institution - 0023, Barcelona

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY

NCT05556343 - A Study to Evaluate the Efficacy, Safety, and Tolerability of MYK-224 in Participants With Symptomatic Obstructive Hypertrophic Cardiomyopathy | Biotech Hunter | Biotech Hunter