Defactinib

Generic Name
Defactinib
Brand Names
-
Drug Type
Small Molecule
Chemical Formula
C20H21F3N8O3S
CAS Number
1073154-85-4
Unique Ingredient Identifier
53O87HA2QU
Background

Defactinib has been investigated for the treatment of Malignant Pleural Mesothelioma.

Associated Conditions
-
Associated Therapies
-
biospace.com
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Verastem Oncology Provides a Clinical Update for RAMP 203 Trial in Advanced KRAS

Verastem Oncology reports no dose-limiting toxicities in RAMP 203 Phase 1/2 study of avutometinib, sotorasib, and defactinib for KRAS G12C mutant NSCLC. Two of three patients showed initial tumor reductions of at least 20%. Enrollment continues, with an interim update planned for 2025.
investing.com
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Verastem's SWOT analysis: cancer drug developer's stock faces pivotal year

Verastem, Inc. focuses on avutometinib for low-grade serous ovarian cancer, with potential FDA approval by mid-2025. The drug shows superior performance in KRAS mutant cases, though efficacy in KRAS wild-type patients is limited. Analysts predict price targets from $7 to $15 per share, with current trading below Fair Value.
ajmc.com
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Avutometinib With Defactinib for Recurrent KRAS Mutant LGSOC Completes Rolling New

The NDA for avutometinib and defactinib in recurrent KRAS mutant LGSOC is complete, aiming for FDA approval in mid-2025. This combination could be the first FDA-approved treatment for this rare, fatal ovarian cancer.
biospace.com
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Verastem Oncology Reports Third Quarter 2024 Financial Results and Highlights Recent

Verastem Oncology completed NDA submission for avutometinib and defactinib in KRAS mutant low-grade serous ovarian cancer, seeking accelerated approval and priority review. Positive safety and efficacy results from the RAMP 201 trial were presented at IGCS 2024. The company anticipates an FDA decision on the NDA by mid-2025 and is preparing for a potential U.S. launch.
pharmabiz.com
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Verastem Oncology submits NDA to US FDA for avutometinib plus defactinib to treat ...

Verastem Oncology completed its NDA submission to the FDA for avutometinib and defactinib, potential first-in-class treatments for recurrent KRAS mutant low-grade serous ovarian cancer (LGSOC). The combination aims to address significant unmet medical need, with preliminary data showing a 44% overall response rate and 22-month median progression-free survival. If approved, it would be the first FDA-approved treatment specifically for this rare cancer, with a potential decision expected by mid-2025.
oncnursingnews.com
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NDA Filed for Avutometinib Plus Defactinib for Low-Grade Serous Ovarian Cancer

FDA received NDA for avutometinib plus defactinib for recurrent KRAS-mutant low-grade serous ovarian cancer. Phase 2 RAMP 201 trial data showed 44% ORR in KRAS-mutant patients and 31% in overall population. Median PFS was 22 months in KRAS-mutant and 12.8 months in KRAS wild-type patients. Verastem Oncology aims for potential FDA approval by mid-2025.
onclive.com
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FDA Approval Sought for Avutometinib Plus Defactinib in Recurrent KRAS+ Low-Grade

The FDA received a rolling NDA for avutometinib and defactinib to treat recurrent KRAS-mutant low-grade serous ovarian cancer. The NDA is supported by the phase 2 RAMP 201 trial data, showing a 44% ORR in KRAS-mutant patients and 31% in the overall population. The combination aims to change the treatment paradigm for this cancer type, with potential FDA approval planned for mid-2025.

Verastem Oncology submits NDA for ovarian cancer treatment

Verastem Oncology completed the rolling NDA submission to the FDA for avutometinib and defactinib combination therapy for low-grade serous ovarian cancer, seeking priority review. The submission is based on Phase II RAMP 201 study results showing a 44% overall response rate and 22-month median progression-free survival in KRAS mutant patients. The treatment received breakthrough therapy and orphan drug designations.
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