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SRRK
Scholar Rock, Inc.distress 2/10 · well-funded / low risk$47.75-1%today-18% from 52w high
Metabolic / Obesity 1Oncology 1
Lead: spinal muscular atrophy · target GLP-1/GIP
Revenue
pre-revenue
Liquidity
$480M
Runway
1.6 yrs
Shares 1y
+25%
Price & events
-0.0% over 6M
CatalystRating changeDilutionFinancingdashed = today
-1.1%
1D
-7.7%
1W
-6.9%
1M
+0.6%
3M
+7.8%
6M
+20.2%
1Y
+419.0%
2Y
+46.2%
5Y
+1.8%
All
Overview
- Market Cap
- $5.72B
- Enterprise Value
- $5.49B
- Volume
- 129.72K
- 52 Week Range
- $27.92 – $57.94
- Total Shares
- 119.83M
- Float Shares
- 91.82M
- Short %
- 19.22%
- % Held by Insiders
- 0.78%
- % Held by Institutions
- 117.14%
- RVOL
- 0.08x
- Beta
- 0.68
Pipeline stages · 2 programs
Apitegromab, Nusinersen, Risdiplam
Preclin›
Ph1›
Ph2›
Ph3›
Filed›
PDUFA›
Approved
SRK-181, anti-PD-(L)1 antibody therapy
Preclin›
Ph1›
Ph2›
Ph3›
Filed›
PDUFA›
Approved
Pipeline · 5 trials · 3 upcoming
| Readout | Phase | Drug | Indication | Enroll | Status |
|---|---|---|---|---|---|
| 2026-11-01 Estimated 50% readout ~2027-01-15 | Phase 3 | Apitegromabfast trackorphanrare pediatricpriority review | Spinal Muscular Atrophy, Spinal Muscular Atrophy Type 3, Spinal Muscular Atrophy Type 2, SMA, Neuromuscular Diseases, Muscular Atrophy, Atrophy, Muscular Atrophy, Spinal, Neuromuscular Manifestations, Anti-myostatin | — | active not recruiting |
| 2028-06 Estimated 50% readout ~2028-07-16 | Phase 2 | Apitegromabfast trackorphanrare pediatricpriority review | Facioscapulohumeral Muscular Dystrophy, FSHD | — | not yet recruiting |
| 2028-11 Estimated 50% readout ~2028-12-16 | Phase 2 | Apitegromab, Nusinersen, Risdiplamfast trackorphanrare pediatricpriority review | Spinal Muscular Atrophy, SMA, Spinal Muscular Atrophy Type 2, Spinal Muscular Atrophy Type 3, Neuromuscular Manifestations, Anti-myostatin | — | recruiting |
| 2025-04-14 | Phase 1 | SRK-181, anti-PD-(L)1 antibody therapy | Cancer | 112 | completed |
| 2025-03-04 | Phase 2 | Apitegromab, Placebo, Tirzepatidefast trackorphanrare pediatricpriority review | Overweight and Obesity | 102 | completed |
Upcoming readouts & decisions · our signals
1 upcoming event has our read — the sell-the-news timing call plus an experimental clinical estimate. Go Pro to see them.
Catalyst news & presentations · 22
- 2026Guided 40%regulatory submissionFiled (NDA/BLA)apitegromab · Anticipated resubmission of biologics license application.SEC 8-K
- second half of 2026Guided 55%readoutPhase 1SRK-439 · Topline data from Phase 1 study expected in H2 2026SEC 8-K
- September 30, 2026Confirmed 100%PDUFAPDUFAapitegromab · PDUFA action date for BLASEC 8-K
- 2026-08-06Estimated 45%earningsEarningsEarnings releaseyahoo
- mid-2026trial initiationsecondaryPhase 2apitegromab · Phase 2 FORGE trial initiation expected mid-2026SEC 8-K
- near mid-2026chmp opinionCHMP (EU)apitegromab · EU MAA decision anticipatedSEC 8-K
- within 30 daysfiling acceptanceFiled (NDA/BLA)apitegromab · FDA acceptance of resubmitted BLA expected within 30 days of March 31, 2026 submission.SEC 8-K
- 2026-03-03partnershipSecured new debt facility of up to $550 million from Blue Owl CapitalSEC 8-K
- 2026-03-03fda agreementapitegromab · Type C meeting resulted in FDA alignment to include second fill-finish facility in BLA resubmission.SEC 8-K
- second half of 2025regulatory submissionFiled (NDA/BLA)SRK-439 · IND filing for SRK-439SEC 8-K
- Q4 2025trial initiationsecondaryPhase 1SRK-439 · Initiate dosing of SRK-439 in healthy volunteers.SEC 8-K
- year-end 2025trial initiationsecondaryapitegromab · Initiate clinical development in a second neuromuscular disorder.SEC 8-K
- 2025-11-14partnershipFiled prospectus supplement for ATM offering of up to $200M common stock through JefferiesSEC 8-K
- 2025-11-12fda agreementapitegromab · Completed constructive in-person Type A meeting with FDA; Catalent confirmed reinspection ready by end of 2025.SEC 8-K
- Q3 2025regulatory submissionFiled (NDA/BLA)SRK-439 · IND application expected to be filedSEC 8-K
- Q3 2025trial initiationsecondaryPhase 2apitegromab · Initiation of Phase 2 OPAL trial in infants and toddlersSEC 8-K
- 3Q 2025trial initiationsecondarySRK-439 · IND submission for SRK-439SEC 8-K
- 2025-09-23crlapitegromab · Complete Response Letter due to manufacturing observations at Catalent IndianaSEC 8-K
- September 22, 2025PDUFAPDUFAapitegromab · PDUFA target action date for BLASEC 8-K
- June 2025readoutPhase 2apitegromab · Topline data from Phase 2 EMBRAZE trialSEC 8-K
- 1Q 2025regulatory submissionFiled (NDA/BLA)apitegromab · BLA and MAA submission for SMASEC 8-K
- March 19, 2025conferencedata presentationsecondaryapitegromab · SAPPHIRE trial data and DMD preclinical data at MDA ConferenceSEC 8-K
Approved drugs (0)
- none — clinical-stage
Capital structure — dilution & financing
🔒 Top holders — Pro
Institutional ownership + quarter-over-quarter accumulation/trimming.
Upgrade to ProWall St ratings
strong buy · target $59 (+24% upside) · 16 analysts
- 2026-07-21WedbushOutperform
- 2026-05-08HC Wainwright & Co.Buy
- 2026-05-08BarclaysOverweight
- 2026-04-21Canaccord GenuityBuy
- 2026-04-01WedbushOutperform
- 2026-03-16JP MorganOverweight
Competitors — GLP-1/GIP
Recent news
- 2026-07-21Scholar Rock says EU opinion on SMA drug may be pushed to later in 2026 - Reuters
- 2026-07-20Law firm investigates Scholar Rock officers for possible shareholder duty breaches - Pluang
- 2026-07-20Scholar Rock awaits FDA decision on apitegromab EU approval - Investing.com UK
- 2026-07-20Scholar Rock Provides Update on Timing of Committee for Medicinal Products for Human Use (CHMP) Opinion for Apitegromab Marketing Authorisation Application (MAA) for Spinal Muscular Atrophy (SMA) - Business Wire
- 2026-07-1711 New Hires Get Scholar Rock Equity Awards Covering 118,586 Shares - Stock Titan
- 2026-07-17Scholar Rock Reports New Employee Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) - Business Wire
- 2026-07-16Scholar Rock (SRRK) Goldman Sachs 47th Annual Global Healthcare Conference 2026 summary - Quartr
- 2026-07-16Scholar Rock (SRRK) Q3 2025 earnings summary - Quartr
Not financial advice. Data: ClinicalTrials.gov, SEC EDGAR, FINRA, Nasdaq, Yahoo.