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.
Verastem Oncology (Nasdaq: VSTM) reported positive interim results and ongoing advancements in its recurrent low-grade serous ovarian cancer (LGSOC) program. The combination therapy of avutometinib and defactinib demonstrated a confirmed objective response rate of 28% among 29 evaluable patients. The company's cash position improved to $87.9 million as of December 31, 2022, with a pro-forma estimate of $117.9 million post a $30 million funding from a Series B convertible preferred stock sale. Despite a net loss of $73.8 million for the full year, the firm remains focused on regulatory approval pathways and expanding clinical trials for RAS pathway-driven cancers.
Verastem Oncology (Nasdaq: VSTM) has made significant strides in advancing its lead compound, avutometinib, for treating recurrent low-grade serous ovarian cancer (LGSOC). The positive interim results from the RAMP 201 trial prompted plans for a confirmatory study, aiming for FDA accelerated approval in 2023. The company has strengthened its financial position, securing up to $150 million in non-dilutive financing and $60 million through a private placement. Upcoming milestones include data read-outs for other RAS pathway-driven cancers and continued enrollment in trials, enhancing its pipeline potential.
Verastem Oncology (Nasdaq: VSTM) has announced a private placement to sell approximately 2.1 million shares of Series B Convertible Preferred Stock, aiming to raise about
Verastem Oncology (Nasdaq: VSTM) has announced positive interim results from the RAMP 201 Phase 2 study evaluating avutometinib combined with defactinib for treating recurrent low-grade serous ovarian cancer (LGSOC). The combination demonstrated a confirmed objective response rate (ORR) of 28%, with a high disease control rate of 93%. The company plans to file for accelerated approval based on mature data and discussions with the FDA. Target enrollment has been achieved, and the safety profile showed no new signals, with most adverse effects being mild to moderate.
Verastem Oncology (Nasdaq: VSTM) announced the grant of 96,700 restricted stock units (RSUs) to four new employees as part of its recruitment strategy. These RSUs, granted under the Nasdaq inducement grant exception, will vest 25% on each employee's one-year anniversary, with the remaining shares vesting quarterly over three years, contingent on continued employment. Verastem focuses on developing novel small molecule drugs targeting critical cancer cell survival pathways, including RAF/MEK and FAK inhibition, aiming to enhance the lives of cancer patients.
Verastem Oncology (Nasdaq: VSTM) has appointed Robert Gagnon to its Board of Directors, effective December 13, 2022. Gagnon, previously Chief Financial Officer at Verastem, brings over 20 years of financial expertise. His role aims to enhance the company's strategic goals, particularly in treating low-grade serous ovarian cancer and RAS-driven tumors. Verastem's investigational drug, avutometinib, is in late-stage development, having received Breakthrough Therapy designation from the FDA for LGSOC treatment, indicating its potential significance in addressing unmet medical needs.
Verastem Oncology (Nasdaq: VSTM) reported its Q3 2022 financial results, highlighting advancements in its RAMP program for Avutometinib (VS-6766) targeting RAS pathway-driven tumors. The RAMP 201 trial showed encouraging interim results, paving the way for a Q4 meeting with the FDA to discuss treatment regimens for low-grade serous ovarian cancer. The company ended the quarter with $104 million in cash and reported a net loss of $18.1 million. Operating expenses increased to $17.7 million due to higher R&D costs, while non-GAAP adjusted net loss was $16.6 million.
Verastem Oncology (Nasdaq: VSTM) has appointed Anil Kapur to its Board of Directors, effective October 20, 2022. Mr. Kapur brings over 25 years of experience in oncology and commercial operations, having held senior roles at Geron Corporation, Actinium Pharmaceuticals, and Bristol-Myers Squibb. His expertise will be pivotal as Verastem advances its lead compound, VS-6766, which is currently in late-stage development for recurrent low-grade serous ovarian cancer. The company is also conducting several clinical trials involving this compound in various cancer types.
Verastem Oncology (Nasdaq: VSTM) announced the granting of stock options for 22,500 shares and 15,000 restricted stock units (RSUs) to a new employee. These awards were issued under the Nasdaq inducement grant exception, aligning with Nasdaq Listing Rule 5635(c)(4). The exercise price of the stock options is
Verastem Oncology (Nasdaq: VSTM) has announced updates on its RAMP clinical trials. The RAMP 201 trial for recurrent low-grade serous ovarian cancer (LGSOC) shows promising results, prompting an FDA meeting in Q4 to discuss regulatory paths. Conversely, the RAMP 202 trial for KRAS G12V-mutant non-small cell lung cancer (NSCLC) did not meet criteria for continuation, with an overall response rate of only 11%. Ongoing trials RAMP 203 and RAMP 204 are progressing, and newly issued patents extend coverage of VS-6766 and its combinations to 2038 and 2040.