Welcome to our dedicated page for Foghorn Therapeutics news (Ticker: FHTX), a resource for investors and traders seeking the latest updates and insights on Foghorn Therapeutics stock.
Foghorn Therapeutics Inc. (FHTX) is a clinical-stage biopharmaceutical pioneer developing precision medicines targeting chromatin regulation in oncology. This news hub provides investors and industry professionals with essential updates on the company's therapeutic pipeline, strategic collaborations, and clinical milestones.
Access timely reports on FHTX's innovative programs including FHD-286 (hematologic cancers), FHD-609 (synovial sarcoma), and FHD-909 (non-small cell lung cancer). Stay informed about regulatory developments, partnership announcements, and scientific presentations related to their Gene Traffic Control platform.
Our curated news collection serves as a comprehensive resource for tracking progress across preclinical studies, clinical trials, and business operations. Bookmark this centralized source for verified updates on Foghorn's novel protein degraders and chromatin-targeting therapies.
Foghorn Therapeutics Inc. (Nasdaq: FHTX), a clinical stage biotech firm, will participate in the Bank of America 2022 Precision Oncology Conference on October 3, 2022, at 12:20 p.m. ET. The company's innovative Gene Traffic Control platform aims to address gene expression issues in serious diseases, with a primary focus on oncology. A webcast of the event will be available on their website for 90 days post-event. Foghorn is developing several oncology product candidates, with two currently in clinical trials.
Foghorn Therapeutics (Nasdaq: FHTX) has announced management's participation in key investor conferences this September. The biotechnology company focuses on developing innovative treatments by correcting abnormal gene expression, particularly in oncology. The upcoming conferences include the Morgan Stanley 20th Annual Global Healthcare Conference on September 12 and the H.C. Wainwright 24th Annual Global Investment Conference on September 13. Webcasts of these events will be available on their website for 90 days post-conference.
Foghorn Therapeutics has announced the appointment of co-founder Cigall Kadoch as an Investigator for the Howard Hughes Medical Institute (HHMI), effective September 6, 2022. Following this appointment, Dr. Kadoch has resigned from her position on Foghorn’s Board of Directors but will continue as a Scientific Advisor to the Board. CEO Adrian Gottschalk praised her contributions, emphasizing her leadership in chromatin regulation research. Foghorn continues to focus on developing innovative therapies for serious diseases through its Gene Traffic Control platform.
Foghorn Therapeutics (Nasdaq: FHTX) announced a full clinical hold by the FDA on the Phase 1 study of its drug FHD-286 for acute myelogenous leukemia (AML) and myelodysplastic syndrome (MDS). This decision arose from reports of additional suspected fatal differentiation syndrome cases linked to FHD-286. Meanwhile, the study for metastatic uveal melanoma is proceeding as planned, with data expected in early 2023. Foghorn remains committed to addressing FDA concerns to lift the hold promptly.
Foghorn Therapeutics (Nasdaq: FHTX) announced the election of B. Lynne Parshall to its Board as the Chair of the Audit Committee. With nearly 30 years in biotechnology and experience at Ionis Pharmaceuticals, her leadership is expected to bolster Foghorn's growth. CEO Adrian Gottschalk emphasized that her track record in therapy development will be pivotal as the company works towards its vision of a fully-integrated biotech. Parshall will play a crucial role in advancing key clinical programs, including FHD-286 and FHD-609.
Foghorn Therapeutics (FHTX) provided a corporate and financial update for Q2 2022. The Phase 1 study of FHD-286 in metastatic uveal melanoma is progressing, while a partial clinical hold by the FDA affects its use in AML and MDS. Initial clinical data for FHD-609 in synovial sarcoma is expected in 2023. The company achieved a research milestone under its Merck collaboration, triggering a $5 million payment. As of June 30, 2022, Foghorn reported $394.7 million in cash and equivalents, indicating strong financial health.
Foghorn Therapeutics (Nasdaq: FHTX) announced its participation in key investor conferences throughout August 2022, focusing on oncology and the innovative Gene Traffic Control platform. Key events include virtual meetings on August 8 and a panel discussion at the 13th Annual Wedbush PacGrow Healthcare Conference on August 9 at 10:20 a.m. ET. Foghorn is advancing a pipeline of drug candidates that target genetically determined dependencies, with two currently in clinical studies. A webcast of the panel will be available for up to 90 days after the event.
Foghorn Therapeutics (Nasdaq: FHTX) has announced its participation in three upcoming investor conferences. The focus is on its Gene Traffic Control® Platform, which aims to innovate oncology treatments. Key events include:
- Cowen's 3rd Annual Oncology Innovation Summit on June 2 at 10:30 a.m. ET.
- Jefferies Healthcare Conference on June 8 at 1:30 p.m. ET.
- Goldman Sachs 43rd Annual Global Healthcare Conference on June 13 at 3:20 p.m. PT.
Webcasts will be available via the company's website post-event.
Foghorn Therapeutics (Nasdaq: FHTX) announced that the FDA has placed a partial clinical hold on its Phase 1 study of FHD-286 in patients with acute myelogenous leukemia (AML) and myelodysplastic syndrome (MDS), following a report of a death linked to potential differentiation syndrome. While existing patients can continue treatment, new patient enrollment is halted until the issue is resolved. This hold does not affect the ongoing FHD-286 study for metastatic uveal melanoma. The company is suspending guidance on data release timing for the AML/MDS study.
Foghorn Therapeutics (FHTX) continues to advance its pipeline with three phase 1 studies targeting the chromatin regulatory system. Initial clinical data for FHD-286 is anticipated in H2 2022, focusing on cancers such as AML and uveal melanoma, while FHD-609 aims for data in 2023. Recent preclinical findings at AACR highlight FHD-286's anti-tumor activity. The company reported a strong balance sheet with $424.7 million in cash as of March 31, 2022, supporting ongoing development efforts.