IQVIA and Flagship Pioneering Announce Strategic Collaboration to Accelerate the Development of Breakthrough Life Sciences Companies
Collaboration Announcement: IQVIA and Flagship Pioneering have formed a strategic partnership aimed at accelerating the development of innovative life sciences companies by leveraging IQVIA's extensive capabilities in clinical research and analytics.
Focus Areas: The collaboration will concentrate on three main service areas: drug development strategy and analytics, clinical development, and asset valuation and due diligence to enhance efficiency in drug development.
Mission Alignment: Both companies emphasize their commitment to improving patient outcomes and advancing healthcare innovations, with IQVIA aiming to bring better treatments to patients faster through this partnership.
Flagship Ecosystem: Flagship Pioneering has created over 40 biopharma companies since its inception, showcasing significant value creation in the life sciences sector, supported by IQVIA's robust data infrastructure and analytics.
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- Summit Participation: Foghorn Therapeutics will participate in the Guggenheim Emerging Outlook Biotech Summit on February 11-12, 2026, in New York, showcasing its innovative drug development in oncology.
- Management Presentation: CEO Adrian Gottschalk is scheduled to present on February 11 at 3:00 PM EST, sharing the latest advancements in the company's gene expression correction efforts, which is expected to attract investor interest.
- Webcast Availability: The presentation will be webcasted under the 'Events & Presentations' section of the company's website and will be available for replay for 30 days, enhancing investor engagement.
- R&D Platform: Foghorn's Gene Traffic Control® platform focuses on developing drug candidates targeting genetically determined dependencies, aiming to drive therapeutic innovation in oncology with significant market potential.

- FDA Orphan Drug Designation: Atossa Therapeutics (ATOS) announced that its (Z)-endoxifen received Orphan Drug Designation from the FDA, leading to a 12.98% stock increase to $0.69, marking a significant milestone in the treatment of Duchenne muscular dystrophy and expected to drive future R&D progress.
- Clinical Trial Progress: ImmunityBio (IBRX) reported that over 85% of the study population has been enrolled in its registrational trial QUILT-2.005 for BCG-naïve non-muscle-invasive bladder cancer, with stock rising 9.43% to $6.04, and full enrollment anticipated by Q2 2026, enhancing market confidence.
- NASDAQ Compliance Extension: Femasys (FEMY) received NASDAQ approval for a 180-day extension to meet the minimum $1.00 bid price requirement, with stock climbing 10.68% to $0.72, providing the company until July 13, 2026, to regain compliance, alleviating investor concerns.
- Successful Financing: Foghorn Therapeutics (FHTX) closed a $50 million registered direct financing at a 30% premium, resulting in a 4.02% stock increase to $6.26, demonstrating market confidence and support for its future development.

- Market Growth Potential: The precision oncology market is projected to surge from $110 billion to $225.65 billion, highlighting the industry's urgent demand for registration-ready assets, positioning Oncolytics Biotech at the forefront of this growth wave.
- Executive Appointments: Oncolytics Biotech has appointed John McAdory as Executive Vice President of Strategy and Operations and Yujun Wu as Vice President, Head of Biostatistics, both bringing extensive experience in late-stage oncology trial execution and regulatory strategy to drive the company's registration-directed programs in gastrointestinal cancers.
- Clinical Data Breakthrough: In third-line data for anal cancer, pelareorep achieved a 29% objective response rate, nearly tripling historical benchmarks, with a median duration of response reaching approximately 17 months, showcasing its potential in a setting with no FDA-approved treatment options.
- FDA Study Design Approval: Oncolytics has secured FDA alignment on its Phase 3 study design for first-line metastatic pancreatic cancer, positioning it to launch the only immunotherapy registration trial currently planned for this disease, further solidifying its market position.

- Market Growth Potential: The precision oncology market is projected to surge from $110 billion to $225.65 billion, highlighting the industry's urgent need for registration-ready assets, positioning Oncolytics Biotech as a key investment opportunity.
- Executive Appointments: Oncolytics Biotech has appointed John McAdory as Executive Vice President of Strategy and Operations and Yujun Wu as Vice President, Head of Biostatistics, both bringing extensive experience in late-stage oncology trial execution and regulatory strategy, which will drive the company's registration programs in gastrointestinal cancers.
- Clinical Data Breakthrough: Pelareorep achieved a 29% objective response rate in third-line treatment, nearly tripling historical benchmarks in a setting with no FDA-approved treatment options, indicating significant clinical potential and likely accelerating the approval process for anal cancer.
- FDA Study Design Endorsement: Oncolytics has secured FDA alignment on its Phase 3 study design for pelareorep in first-line metastatic pancreatic cancer, marking the company's unique position in the immunotherapy registration trial landscape and expected to drive future market opportunities.
- Successful Financing: Foghorn Therapeutics secured $50 million in equity financing with investors including BVF Partners, expected to close on January 13, 2026, at a price of $6.71 per share, representing a 30% premium to the January 9 closing price, providing robust funding for future R&D initiatives.
- Strong Financial Position: Post-financing, the company anticipates cash and cash equivalents to reach approximately $208.9 million, ensuring continued investment in its pipeline over the next two years, particularly for the FHD-909 project targeting SMARCA4-mutant cancers.
- Clinical Trial Progress: The Phase 1 dose-escalation trial of FHD-909 is advancing as planned, primarily targeting patients with non-small cell lung cancer, which is expected to offer new treatment options in this high-need area and improve patient prognosis.
- Drug Development Outlook: Foghorn's selective CBP and EP300 degrader programs are on track to be IND-ready in 2026, demonstrating potential applications in ER+ breast cancer and hematologic malignancies, further solidifying the company's innovative position in oncology treatment.
- Successful Financing: Foghorn Therapeutics has secured $50 million in equity financing with investors including BVF Partners, expected to close on January 13, 2026, at a 30% premium, reflecting strong investor confidence in the company's strategic vision.
- Strong Financial Position: Post-financing, the company anticipates having approximately $208.9 million in cash and equivalents, ensuring continued investment in its pipeline and extending its cash runway into the first half of 2028, thereby enhancing its viability in the competitive biotech landscape.
- Clinical Trial Progress: The Phase 1 dose-escalation trial of FHD-909 is advancing as planned, targeting patients with SMARCA4-mutant non-small cell lung cancer, which is expected to provide new treatment options and address significant unmet medical needs in this area.
- Drug Development Outlook: Foghorn's selective CBP and EP300 degrader programs are on track to be IND-ready in 2026, showcasing the company's innovative potential in oncology and the possibility of transforming existing treatment paradigms.




