Clinical Trials
2
Trial Phases
1 Phases
Drug Approvals
0
Drug Approvals
No drug approvals found
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Clinical Trials
Distribution across different clinical trial phases (2 trials with phase data)• Click on a phase to view related trials
A Safety and Efficacy Study Evaluating CTX112 in Adult Subjects With Refractory Autoimmune Disease
- Conditions
- SLE (Systemic Lupus)Systemic SclerosisLupus Erythematosus, SystemicLupus NephritisInflammatory Myopathy, IdiopathicMyositisDiffuse Cutaneous Systemic Sclerosis
- Interventions
- First Posted Date
- 2025-04-13
- Last Posted Date
- 2025-08-12
- Lead Sponsor
- CRISPR Therapeutics
- Target Recruit Count
- 80
- Registration Number
- NCT06925542
- Locations
- 🇺🇸
Research Site 4, Redwood City, California, United States
🇺🇸Research Site 2, Chicago, Illinois, United States
🇺🇸Research Site 8, Iowa City, Iowa, United States
A Safety and Efficacy Study Evaluating CTX131 in Adult Subjects With Relapsed/Refractory Hematologic Malignancies
- Conditions
- Acute Myeloid LeukemiaT Cell LymphomaB Cell Lymphoma
- Interventions
- First Posted Date
- 2024-07-09
- Last Posted Date
- 2025-06-29
- Lead Sponsor
- CRISPR Therapeutics
- Target Recruit Count
- 290
- Registration Number
- NCT06492304
- Locations
- 🇦🇺
Research Site 7, East Melbourne, Victoria, Australia
🇺🇸Research Site 6, Phoenix, Arizona, United States
🇺🇸Research Site 5, Stanford, California, United States
News
ToolGen Files Patent Infringement Lawsuit Against Lonza Over CRISPR Technology Used in CASGEVY Production
ToolGen has filed a patent infringement lawsuit in the Netherlands against Lonza, alleging unauthorized use of its CRISPR-Cas9 RNP technology in producing CASGEVY, the world's first approved gene-editing therapy.
Vertex Pharmaceuticals Partners with Enlaza Therapeutics in $45 Million Deal to Develop Autoimmune and Gene-Editing Therapies
Vertex Pharmaceuticals has committed $45 million upfront to partner with Enlaza Therapeutics, with potential total deal value exceeding $2 billion for autoimmune disease treatments.
Follicular Lymphoma Market Poised for 6% CAGR Growth Through 2034 as Novel Therapies Advance
The follicular lymphoma market is projected to grow at a 6% CAGR during 2025-2034, driven by increased disease awareness and rising number of clinical trials focused on this slow-growing B-cell malignancy.
Anti-GPC3 Targeted Therapies Market Expands with Novel Treatment Approaches for Hepatocellular Carcinoma
The anti-GPC3 targeted therapies market is expected to surge significantly by 2040, driven by increasing cancer incidence and clinical pipeline activity across hepatocellular carcinoma, non-small cell lung cancer, and gastric cancer.
CRISPR Therapeutics' CTX310 Shows Promising Lipid Reduction Results in Phase 1 Trial
CRISPR Therapeutics' CTX310, an in vivo ANGPTL3 knockout therapy, demonstrated peak reductions of up to 82% in triglycerides and 86% in LDL cholesterol at dose level four in Phase 1 trial results.
Oruka Therapeutics Promotes Laura Sandler to COO as Company Advances Novel Psoriasis Pipeline
Oruka Therapeutics has promoted Laura Sandler to Chief Operating Officer, leveraging her 20+ years of biopharmaceutical experience including her role in advancing CRISPR's first approved therapy exa-cel.
CRISPR Therapeutics Reports Breakthrough Results from In Vivo Gene Therapy CTX310 for Heart Disease
CRISPR Therapeutics reported initial top-line results from an early-stage study on CTX310, showing peak reductions of up to 82% in triglycerides and 81% in LDL cholesterol with a single dose.
Tourmaline Bio's Heart Disease Antibody Shows Promise in Phase 2, But Shares Fall Amid Competition Concerns
Tourmaline Bio's antibody drug pacibekitug demonstrated significant reduction in cardiovascular risk biomarkers compared to placebo in Phase 2 trials, but shares fell 18% as investors question its competitive edge against Novo Nordisk's offering.
CRISPR Therapeutics Expands into siRNA Therapies with $95M Sirius Partnership for Thromboembolic Disorders
CRISPR Therapeutics is diversifying beyond gene editing through a strategic $95 million partnership with Sirius Therapeutics to develop SRSD107, a long-acting siRNA therapy targeting Factor XI for thromboembolic disorders.
FDA Clears Capsida's Revolutionary IV Gene Therapy for STXBP1-DEE, First to Cross Blood-Brain Barrier
Capsida Biotherapeutics has received FDA IND clearance for CAP-002, the first intravenously administered gene therapy that crosses the blood-brain barrier while avoiding off-target tissues for STXBP1-DEE.