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Verastem - VSTM STOCK NEWS

Welcome to our dedicated page for Verastem news (Ticker: VSTM), a resource for investors and traders seeking the latest updates and insights on Verastem stock.

Verastem Oncology (NASDAQ: VSTM) is a clinical-stage biopharmaceutical company pioneering targeted therapies for cancer treatment, with a specialized focus on inhibiting RAF/MEK and FAK signaling pathways. This dedicated news hub provides investors and industry observers with timely updates on the company's progress in developing innovative solutions for treatment-resistant cancers.

Access comprehensive coverage of Verastem's latest developments including clinical trial milestones, regulatory updates, strategic partnerships, and financial results. Our curated news collection serves as an essential resource for tracking advancements in cancer stem cell research and precision oncology programs.

Find authoritative reporting on key initiatives such as VS-6766 (RAF/MEK inhibitor) developments, combination therapy trials, and intellectual property updates. The page consolidates earnings announcements, research publications, and management commentary for efficient due diligence.

Bookmark this page for direct access to verified information about Verastem's pipeline progress and corporate developments. Check regularly for new updates on therapeutic candidates moving through clinical evaluation and their potential implications for cancer care innovation.

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Verastem Oncology (VSTM) reports progress in developing combination therapies for cancer, including Phase 3 trials and FDA Fast Track designation. Financial results for Q4 2023 and full year released.
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Verastem Oncology (Nasdaq: VSTM) presented multiple oral and poster presentations at the SGO 2024 Annual Meeting on Women’s Cancer. The presentations included a late-breaking oral presentation of avutometinib and defactinib combination data from the RAMP 201 Part A trial in heavily pretreated patients with low-grade serous ovarian cancer.
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Verastem Oncology receives FDA Orphan Drug Designation for avutometinib and defactinib in recurrent low-grade serous ovarian cancer, aiming for Accelerated Approval in 2024. The company is addressing a rare cancer with no approved treatments, impacting a significant patient population.
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Verastem Oncology announces promising preclinical data on GFH375 (VS-7375) and avutometinib-FAK inhibitor combination for pancreatic and colorectal cancer treatment. Partner GenFleet to submit IND in H1 2024. Key presentations at AACR Annual Meeting 2024.
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Verastem Oncology (VSTM) plans to submit an NDA for Accelerated Approval for the combination of avutometinib and defactinib in recurrent low-grade serous ovarian cancer in the first half of 2024. They also aim to provide data read-outs with avutometinib and defactinib combinations in KRAS G12C-mutant non-small cell lung cancer and frontline metastatic pancreatic cancer, as well as supporting their collaborator GenFleet in advancing oral KRAS G12D inhibitor GFH375/VS-7375 into a Phase 1 clinical trial this year.
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Verastem Oncology (VSTM) announced that the FDA has granted Fast Track Designation to its investigational RAF/MEK clamp, avutometinib, in combination with Amgen’s KRAS G12C inhibitor, LUMAKRASTM (sotorasib), for the treatment of patients with KRAS G12C-mutant metastatic non-small cell lung cancer (NSCLC). Initial RAMP 203 trial results showed confirmed responses in both KRAS G12C inhibitor resistant and naïve patients. Enrollment is ongoing in the expansion phase, with updated results expected in the first half of 2024.
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Verastem Oncology (VSTM) to participate in fireside chat at B. Riley Securities 4th Annual Oncology Conference on January 18, 2024
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Verastem Oncology (VSTM) Grants Stock Options to New Employees
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Verastem Oncology (Nasdaq: VSTM) plans to submit an Investigational New Drug (IND) for GFH375/VS-7375, an oral inhibitor targeting KRAS G12D, the most prevalent KRAS mutation in human cancer, in the first half of 2024. The potential best-in-class inhibitor is the lead program from Verastem's collaboration with GenFleet Therapeutics. The company aims to address the lack of FDA-approved therapies targeting KRAS G12D, which represents 26% of all KRAS mutations. The collaboration with GenFleet aims to advance three oncology discovery programs related to RAS pathway-driven cancers, with Verastem having the exclusive option to obtain a license to each of the three compounds after successful completion of pre-determined milestones in a Phase 1 trial.
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Verastem Oncology (VSTM) initiates Phase 3 RAMP 301 trial to evaluate avutometinib and defactinib combination for recurrent low-grade serous ovarian cancer. The combination reports an objective response rate of 45% with manageable safety and tolerability profile. The company plans to submit an Accelerated Approval NDA based on mature data from RAMP 201 and FRAME trials.
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Nasdaq:VSTM

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295.55M
46.35M
1.17%
76.29%
13.4%
Biotechnology
Pharmaceutical Preparations
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United States
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