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SW-682 in Advanced Solid Tumors

Address: 1901 East Rd, Houston, TX 77054, USA

Phone: 877-451-7009

Mesothelioma Type:

  • Pleural: True
  • Peritoneal: True
  • Pericardial: True
  • Tunica Vaginalis: True

Type: Epitheliod, Biphasic, Sarcomatoid

Condition: Advanced Solid Tumor, Malignant Mesothelioma

Description: This is a first-in-human (FIH), Phase 1a/1b open-label, multicenter, dose escalation and dose expansion study of SW-682 in adult participants with metastatic or unresectable advanced solid tumors with or without Hippo pathway alterations that are refractory to, or have progressed, during or after appropriate prior systemic anticancer therapy, including chemotherapy, immunotherapy, radiation therapy or targeted therapy, or for which no treatment is available, or prior standard of care (SOC) therapy was not tolerated and for which there is no further SOC treatment available. The study includes a Part 1 (Phase 1a) dose escalation phase and a Part 2 (Phase 1b) dose expansion to optimize the dose to be used for further development. All participants will self-administer SW-682 by mouth in 28-day cycles.

Research Center: MD Anderson Cancer Center

Treatment Interventions: DRUG: SW-682, DRUG: Combination Therapy

Potential Impact: Low

Clinical Trial Number: NCT06251310

Phase: Phase 1

Status: Recruiting

Website: https://clinicaltrials.gov/study/NCT06251310

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