
Search for companies, drugs, and catalysts
Search for companies, drugs, and catalysts
Pharmaceutical Preparations · market cap $9.8B · as of 2026-06-26
Research and calibrated estimates, not financial advice — verify before acting.
| Asset | Phase | Indication |
|---|---|---|
| 250 mg CK-2017357 | Phase 2 | Amyotrophic Lateral Sclerosis |
| CK-2017357 (Part A) | Phase 2 | Amyotrophic Lateral Sclerosis |
| Omecamtiv Mecarbil | Phase 3 | Heart Failure With Reduced Ejection Fraction |
| CK-4021586 (150 mg, 300 mg, 450 mg, and 600 mg) | Phase 2 | Symptomatic Heart Failure With Preserved Ejection Fraction (HFpEF) |
| Aficamten | Phase 3 | Symptomatic Non-Obstructive Hypertrophic Cardiomyopathy |
| CK-2017357 | Phase 2 | Amyotrophic Lateral Sclerosis |
| Omecamtiv Mecarbil Matrix F1 Formulation | Phase 2 | Modified Release Oral Formulation |
| Aficamten (5 mg, 10 mg, 15 mg, and 20 mg) | Phase 3 | Obstructive Hypertrophic Cardiomyopathy (oHCM) |
| Riluzole 50 MG | Phase 2 | Amyotrophic Lateral Sclerosis |
| Standard of Care | Phase 3 | Heart Failure |
| CK-1827452 | Phase 2 | Heart Failure |
| Aficamten (CK-3773274) (5 mg, 10 mg, 15 mg and 20 mg) | Phase 3 | Obstructive Hypertrophic Cardiomyopathy (oHCM) |
| Reldesemtiv | Phase 2 | Amyotrophic Lateral Sclerosis |
| 375 mg CK-2017357 | Phase 2 | Intermittent Claudication |
| Reldesemtiv 150 mg | Phase 2 | Spinal Muscular Atrophy |
| 25 mg Omecamtiv Mecarbil | Phase 2 | Heart Failure With Reduced Ejection Fraction |
| SB-743921 | Phase 2 | Non-Hodgkin's Lymphoma |
| Omecamtiv Mecarbil (OM) | Phase 3 | Heart Failure |
| CK-3773274 (5 - 15 mg) | Phase 2 | Hypertrophic Cardiomyopathy (HCM) |
| tirasemtiv | Phase 3 | Amyotrophic Lateral Sclerosis (ALS) |
Daily closes through 2026-07-01. Realized vol annualized; max drawdown over ~2 years.
The full dossier is a Pro feature
Thesis, bull & bear, the if-approved scenario, financials, smart-money signals and risks — compiled by CeliA. The catalyst path & pipeline above are free.
See ProApproval odds use historical phase base rates; the if-approved scenario is illustrative (see its note). Figures trace to the sources above — verify before acting.
Data from CatalystAlert (ClinicalTrials.gov, SEC EDGAR, openFDA, Financial Modeling Prep). Compiled by CeliA. Not financial advice.