Syndax Partners with WODA to Expand Access to Revuforj
Syndax Pharmaceuticals and the World Orphan Drug Alliance, WODA, announced a collaboration to expand access to the Company's first-in-class menin inhibitor, Revuforj, through a Managed Access Program. The program is being launched in parts of Eurasia, Central and Southeast Europe, Israel, the Middle East and Turkey, Latin America, and Africa. "We are thrilled to partner with WODA to begin expanding access to Revuforj around the globe, further advancing our mission to transform care for cancer patients," said Anjali Ganguli, Ph.D., Chief Strategy Officer at Syndax Pharmaceuticals. "In addition to providing a pathway for patients to access Revuforj in regions where it would otherwise be inaccessible, this program will also allow more physicians to gain valuable firsthand experience with the medicine, supporting our long-term goal to establish Revuforj as a standard of care treatment globally."
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- Global Access Program: Syndax collaborates with WODA to launch a Managed Access Program aimed at expanding access to Revuforj in regions like Eurasia, the Middle East, Latin America, and Africa, potentially benefiting thousands of patients.
- Physician Experience Accumulation: This program not only provides a pathway for patients to access Revuforj but also allows more physicians to gain firsthand experience with the drug, supporting the long-term goal of establishing Revuforj as a standard treatment globally.
- FDA Approval Context: Revuforj is FDA-approved in the U.S. for treating difficult-to-treat acute leukemia, highlighting its significance in blood cancer treatment and expected to enhance Syndax's competitiveness in the global market.
- Role of WODA: WODA will provide Revuforj in over 150 countries, ensuring compliant and patient-focused distribution, further strengthening Syndax's influence in the global drug access landscape.
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- Best New Drug Award: Syndax Pharmaceuticals' Revuforj® was recognized as Best New Drug at the 2025 Scrip Awards, highlighting its excellence in drug development and enhancing the company's reputation in the biopharma industry.
- FDA Approval: Revuforj received FDA approval in November 2024 for treating relapsed or refractory acute leukemia, marking a significant milestone in innovative cancer therapies and is expected to drive sales growth.
- Second Indication Approval: In October 2025, Revuforj was approved by the FDA for treating relapsed acute myeloid leukemia, demonstrating its potential across multiple patient populations and likely attracting increased investor interest.
- Ongoing Clinical Trials: Revuforj is undergoing multiple clinical trials to explore its use in combination with standard therapies, which is expected to further validate its efficacy and expand market share.
- Award Recognition: Syndax's Revuforj® was named Best New Drug at the 2025 Scrip Awards, highlighting its excellence in drug development and reinforcing the company's leadership in innovative cancer therapies.
- FDA Approval: Revuforj received FDA approval in November 2024 for treating relapsed or refractory acute leukemia, marking a significant breakthrough in treatment options and expected to greatly enhance patient care.
- Market Potential: The success of Revuforj not only boosts Syndax's reputation but also has the potential to increase its market share in acute leukemia, particularly among patients with no satisfactory alternative treatments.
- Ongoing Research: Syndax is conducting multiple clinical trials to evaluate the combination of Revuforj with standard therapies, indicating future potential for enhanced efficacy and market expansion.

Syndax Pharmaceuticals Overview: Syndax Pharmaceuticals, Inc. (NASDAQ:SNDX) is recognized as a promising small-cap biotech stock, with analysts highlighting its potential for significant upside.
Recent Financial Performance: In Q3 2025, Syndax reported a 21% revenue increase to $45.9 million, driven by strong sales of its therapies, particularly Revuforj, which gained FDA approval for a broader patient population.
Price Target Adjustment: JPMorgan adjusted its price target for Syndax from $40 to $33 while maintaining an "Overweight" rating, reflecting changes in their models for the SMID-cap biotechnology sector.
Future Projections: The company ended the quarter with $456 million in cash and projected R&D costs of $380 to $385 million for the year, indicating a solid financial position to support ongoing operations and development.

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