CRISPR Therapeutics AG (CRSP) Stock Analysis
Range Bound setup
Healthcare · Biotechnology
Sell if holding. Engine safety override at $53.23: Quality below floor (1.8 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.6/10 and A.R:R 3.5:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 26%; Elevated put/call ratio: 2.32; Below-average business quality.
CRISPR Therapeutics AG develops gene-editing therapies using CRISPR/Cas9 technology, with one approved product — CASGEVY for sickle cell disease and transfusion-dependent beta thalassemia — commercialized jointly with Vertex Pharmaceuticals. Revenue comes entirely from a 40%... Read more
Sell if holding. Engine safety override at $53.23: Quality below floor (1.8 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.6/10 and A.R:R 3.5:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 26%; Elevated put/call ratio: 2.32; Below-average business quality. Chart setup: RSI 53 mid-range, Bollinger mid-band. Score 5.6/10, moderate confidence.
Passes 7/9 gates (favorable risk/reward ratio, clean insider activity, no SEC red flags, news events none recent, earnings proximity 56d clear, semi cycle peak clear, materials cycle peak clear). Fails on weak momentum and death cross (50MA < 200MA). Suitability: aggressive.
About CRISPR Therapeutics AG
About CRISPR Therapeutics AG
CASGEVY, the first approved CRISPR-based gene therapy, received marketing authorizations for sickle cell disease and transfusion-dependent beta thalassemia in the United States, EU, Great Britain, Canada, Switzerland, and six Middle Eastern countries by 2025 year-end. CRISPR Therapeutics AG holds a 40% economic interest in CASGEVY through its Vertex collaboration, but that revenue share was insufficient to cover the company's 40% share of program costs. Cash, equivalents, and marketable securities were approximately $1.975 billion at December 31, 2025, projected sufficient for at least 24 months.
Revenue flows from CRISPR Therapeutics' 40% share of CASGEVY net sales, which Vertex Pharmaceuticals leads in commercializing across approved markets targeting an estimated 60,000 patients with severe sickle cell disease or transfusion-dependent beta thalassemia in the U.S., Canada, Europe, and parts of the Middle East. Prior to 2025, annual CASGEVY program cost exposure was capped at $110.3 million under a deferral provision in the Vertex agreement; that provision expired at the start of 2025, raising the company's cost burden. Beyond hemoglobinopathies, CRISPR Therapeutics is advancing in vivo liver-editing candidates including CTX310 (Phase 1b for ANGPTL3) and CTX340 (for hypertension), a CAR T program featuring zugocabtagene geleucel in Phase 1/2 for autoimmune disease and hematologic malignancies, and an siRNA collaboration with Sirius Therapeutics entered in May 2025. Manufacturing for zugocabtagene geleucel is conducted at the company's internal GMP facility in Framingham, Massachusetts.
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The company's near-term financial trajectory depends on whether CASGEVY commercial uptake can offset the expanded cost burden, and on whether CTX310 or zugocabtagene geleucel can advance to registrational trials. No in vivo gene-editing therapy had been approved in the U.S. or EU as of the 10-K date, subjecting CRISPR Therapeutics' in vivo programs to a novel regulatory pathway without established precedent. The 10-K discloses that CASGEVY program expenses are expected to exceed the company's 40% revenue share for the foreseeable future — a dynamic that, if uptake ramps slower than projected, could require additional capital before the 24-month runway expires.
See also: Healthcare · Biotechnology
From CRISPR Therapeutics AG's most recent 10-K filing, extracted June 9, 2026.
Recent developments
updated 2026-06-15Recent Developments — CRISPR Therapeutics AG
Latest news
- NEWS Bernstein Maintains Market Perform on CRISPR Therapeutics, Raises Price Target to $56 — benzinga May 13, 2026 positive
- NEWS Citigroup Maintains Buy on CRISPR Therapeutics, Raises Price Target to $82 — benzinga May 6, 2026 positive
- NEWS CRISPR Therapeutics Q1 EPS $(1.28) Misses $(1.20) Estimate, Sales $1.458M Miss $2.700M Estimate — benzinga May 4, 2026 negative
Generated 2026-06-15T18:11:46Z.
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Rating Breakdown
3 floor-breakers·2 ceiling hits
Quality below the gate floor. Component breakdown shows what dragged the score down.static
Volatile — 6.1% daily ATR makes tight stops impractical. Position-size conservatively.static
Momentum below the gate floor. Component breakdown shows what dragged the score down.static
Price Targets
Position Sizing
Risk Alerts
Earnings
Verdict History
Frequently Asked Questions
Sell if holding. Engine safety override at $53.23: Quality below floor (1.8 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.6/10 and A.R:R 3.5:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 26%; Elevated put/call ratio: 2.32; Below-average business quality. Chart setup: RSI 53 mid-range, Bollinger mid-band. Prior stop was $49.30. Score 5.6/10, moderate confidence.
Take-profit target: $75.17 (+41.8% upside). Prior stop was $49.30. Stop-loss: $49.30.
Quality below floor (1.8 < 4.0).
CRISPR Therapeutics AG trades at a P/E of N/A (forward -13.0). TrendMatrix value score: 9.0/10. Verdict: Sell.
32 analysts cover CRSP with a consensus score of 3.8/5. Average price target: $84.
What does CRISPR Therapeutics AG do?CRISPR Therapeutics AG develops gene-editing therapies using CRISPR/Cas9 technology, with one approved product —...
CRISPR Therapeutics AG develops gene-editing therapies using CRISPR/Cas9 technology, with one approved product — CASGEVY for sickle cell disease and transfusion-dependent beta thalassemia — commercialized jointly with Vertex Pharmaceuticals. Revenue comes entirely from a 40% share of CASGEVY product sales under the Vertex collaboration, which did not cover program expenses in 2025; cash, equivalents, and marketable securities were approximately $1.975 billion at December 31, 2025.