Cytokinetics 
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12 Trials

   

Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
omecamtiv mecarbil (AMG 423) / Amgen, Servier
2020-003057-30: Omecamtiv Mecarbil Post-trial Access Protocol for Subjects Completing Study 20110203 GALACTIC-HF

Not yet recruiting
3
1286
Europe
Omecamtiv mecarbil, AMG 423, Modified-release tablet
Amgen Inc., Amgen Inc.
Chronic heart failure with reduced ejection fraction, Chronic Heart Failure, Diseases [C] - Cardiovascular Diseases [C14]
 
 
reldesemtiv (CK-2127107) / Astellas, Cytokinetics
COURAGE-ALS, NCT04944784 / 2020-004040-29: A Study to Evaluate the Efficacy and Safety of Reldesemtiv in Patients With Amyotrophic Lateral Sclerosis (ALS)

Terminated
3
486
Europe, Canada, US, RoW
Reldesemtiv, Placebo
Cytokinetics
Amyotrophic Lateral Sclerosis
07/23
07/23
COURAGE OLE, NCT05442775 / 2021-004727-33: A Phase 3, Open-Label Extension of COURAGE-ALS (CY 5031)

Terminated
3
71
Europe, Canada, US, RoW
Reldesemtiv
Cytokinetics, Cytokinetics Inc
Amyotrophic Lateral Sclerosis
06/23
06/23
aficamten (CK-274) / Cytokinetics
SEQUOIA-HCM, NCT05186818 / 2021-003536-92: Efficacy and Safety Trial of Aficamten vs Placebo in Adults With Symptomatic oHCM

Jul 2023 - Dec 2023: Data from SEQUOIA-HCM trial for obstructive hypertrophic cardiomyopathy
Hourglass Apr 2023 - Jun 2023 : Completion of enrollment of SEQUOIA-HCM trial for obstructive hypertrophic cardiomyopathy
Completed
3
282
Europe, US, RoW
CK-3773274 (5 mg, 10 mg, 15 mg and 20 mg), Placebo to match CK-3773274
Cytokinetics, Corxel Pharmaceuticals
Obstructive Hypertrophic Cardiomyopathy (oHCM)
12/23
12/23
MAPLE-HCM, NCT05767346: Phase 3 Trial to Evaluate the Efficacy and Safety of Aficamten Compared to Metoprolol Succinate in Adults With Symptomatic oHCM

Active, not recruiting
3
175
Europe, Canada, US, RoW
Aficamten (CK-3773274) (5 mg, 10 mg, 15 mg and 20 mg), Placebo to match aficamten, Metoprolol succinate (50 mg, 100 mg, 150 mg and 200 mg), Placebo to match metoprolol succinate
Cytokinetics
Obstructive Hypertrophic Cardiomyopathy (oHCM)
07/25
10/25
NCT06116968: An Open-Label Study of Aficamten for Chinese Patients With Symptomatic oHCM

Recruiting
3
44
RoW
Aficamten, CK-3773274
Ji Xing Pharmaceuticals (Shanghai) Co., Ltd.
Obstructive Hypertrophic Cardiomyopathy
03/26
03/26
ACACIA-HCM, NCT06081894: Phase 3 Trial to Evaluate the Efficacy and Safety of Aficamten Compared to Placebo in Adults With Symptomatic nHCM

Recruiting
3
420
Europe, US, RoW
Aficamten, Placebo
Cytokinetics
Symptomatic Non-Obstructive Hypertrophic Cardiomyopathy
06/26
09/26
CEDAR-HCM, NCT06412666: A Study to Evaluate the Effect of Aficamten in Pediatric Patients (Age 12 to <18 Years) With Symptomatic Obstructive Hypertrophic Cardiomyopathy (oHCM).

Recruiting
2/3
40
US
Aficamten, Placebo
Cytokinetics
Pediatric, Symptomatic Obstructive Hypertrophic Cardiomyopathy
12/28
12/28
REDWOOD-OLE, NCT04848506 / 2020-003571-17: Open-label Extension Study to Evaluate the Long-term Safety and Tolerability of Aficamten in Adults With HCM

Feb 2023 - Jun 2023: Data from Cohort 4 of REDWOOD-HCM trial for patients with non-obstructive HCM
Hourglass Aug 2022 - Dec 2022 : Additional data from REDWOOD-OLE trial for patients with hypertrophic cardiomyopathy
Checkmark From REDWOOD-OLE trial for the treatment of hypertrophic cardiomyopathy at HEART FAILURE 2022
May 2022 - May 2022: From REDWOOD-OLE trial for the treatment of hypertrophic cardiomyopathy at HEART FAILURE 2022
Enrolling by invitation
2/3
900
Europe, US, RoW
Aficamten (5 - 20 mg)
Cytokinetics
Symptomatic Hypertrophic Cardiomyopathy (HCM)
03/28
03/28
REDWOOD-HCM, NCT04219826 / 2019-002785-12: Dose-finding Study to Evaluate the Safety, Tolerability, PK, and PD of CK-3773274 in Adults With HCM

Feb 2023 - Jun 2023: Data from Cohort 4 of REDWOOD-HCM trial for patients with non-obstructive HCM
Checkmark Additional data from REDWOOD-HCM for patients with hypertrophic cardiomyopathy at ASE 2022
Jun 2022 - Jun 2022: Additional data from REDWOOD-HCM for patients with hypertrophic cardiomyopathy at ASE 2022
Checkmark Safety and efficacy data from from cohort 3 of REDWOOD-HCM trial
Feb 2022 - Feb 2022: Safety and efficacy data from from cohort 3 of REDWOOD-HCM trial
More
Completed
2
96
Europe, US
CK-3773274 (5 - 15 mg), CK-3773274 (10 - 30 mg), Placebo for CK-3773274
Cytokinetics
Hypertrophic Cardiomyopathy (HCM)
02/23
02/23
NCT05924815: Study to Evaluate the Effect of Aficamten Administration on QT/QTc Interval

Completed
1
44
US
Aficamten, Aficamten-matching Placebo, Moxifloxacin
Cytokinetics
Healthy Participants
11/23
11/23
CK-136 / Cytokinetics
NCT05662215: A Single and Multiple Ascending Dose Study of CK-3828136 in Healthy Adult Participants

Terminated
1
57
US
CK-3828136, Placebo for CK-3828136
Cytokinetics
Healthy Participants
08/23
08/23
CK-271 / Cytokinetics
No trials found
Undisclosed skeletal muscle activators / Cytokinetics
No trials found

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