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Scholar Rock/$SRRK

1D1W1M3M6MYTD1Y5YMAX

About Scholar Rock

Scholar Rock Holding Corp is a biopharmaceutical company focused on improving the lives of children and adults with Spinal Muscular Atrophy and other rare, severe, and debilitating neuromuscular diseases. Its pipeline candidates include apitegromab and a subcutaneous formulation of apitegromab. The clinical-stage pipeline also includes SRK-439, an investigational subcutaneously administered fully human anti-pro/latent myostatin antibody with high inhibitory potency and selectivity toward myostatin, being developed for the treatment of rare neuromuscular diseases. The company also maintains early-stage programs focused on therapies for rare, severe, and debilitating neuromuscular diseases.
Ticker
$SRRK
Sector
Health
Primary listing
NASDAQ
Employees
289

Scholar Rock Metrics

BasicAdvanced
$5.2B
-
-$3.36
0.68
-

What the Analysts think about Scholar Rock

Analyst ratings (Buy, Hold, Sell) for Scholar Rock stock.
Analyst projections of the future price of Scholar Rock stock.

Bulls say / Bears say

The FDA approved ISEMBYLD for adults and children aged two and over with SMA who are on SMN2-targeted treatment. In its pivotal trial, the recommended dose improved motor-function scores by 2.2 points versus placebo, giving Scholar Rock its first commercial product and a differentiated add-on treatment. (Scholar Rock)
Scholar Rock is extending its myostatin programme beyond SMA: its Phase 2 FORGE trial is testing apitegromab in FSHD, while SRK-439 is in a Phase 1 study. Success could open further uses for the company’s muscle-targeting approach. (Scholar Rock)
The company had $492 million in cash and marketable securities at June 30, and FDA approval made a further $150 million loan tranche available. The FDA has also awarded it a rare paediatric disease priority review voucher, giving Scholar Rock another potential source of funding as it builds the launch and develops its pipeline. (Scholar Rock, Federal Register)
Fractures occurred in 9% of patients on the recommended dose versus 2% on placebo. The FDA requires fracture cases to be reported as alerts and a pregnancy safety study, which could keep safety under close scrutiny after launch. (Scholar Rock, SEC)
Early uptake may be slowed by monthly infusions, prior-authorisation requirements and treatment-centre formulary decisions. Management expected access friction in the first few quarters, so the broad FDA label may not translate quickly into sales. (Investing.com)
European expansion faces a separate regulatory and manufacturing hurdle: Scholar Rock withdrew its European application and said it would resubmit it with an alternative manufacturing site. That leaves the timing of approval and sales outside the US uncertain. (Reuters)
Data summarised monthly by Lightyear AI. Last updated on 1 Nov 2026.

Scholar Rock Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

Scholar Rock Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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