What are the implications of PF-06821497 (Mevrometostat) phase 2 results?

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Last updated: December 8, 2025View editorial policy

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PF-06821497 (Mevrometostat) Phase 2 Results

I cannot provide specific information about PF-06821497 (Mevrometostat) phase 2 results, as this agent is not discussed in any of the provided evidence sources.

What the Evidence Shows

The provided literature focuses exclusively on:

  • Multiple myeloma treatment regimens including various combinations of proteasome inhibitors, immunomodulatory drugs, and monoclonal antibodies 1
  • EZH2 inhibitors such as valemetostat and tazemetostat for non-Hodgkin lymphoma, malignant pleural mesothelioma, and rhabdoid tumors 2, 3, 4, 5
  • Myeloproliferative neoplasms and various combination therapies 1

Key Distinction

PF-06821497 (Mevrometostat) is not mentioned in any of the guideline or research evidence provided. While the evidence discusses other EZH1/EZH2 inhibitors (valemetostat achieved a 54.5% overall response rate in relapsed/refractory non-Hodgkin lymphoma 2, and tazemetostat showed activity in B-cell lymphomas and solid tumors 4), these are distinct compounds with different molecular profiles and clinical development programs.

Clinical Context

Without access to the actual phase 2 trial data for PF-06821497, I cannot comment on:

  • The specific indication studied
  • Efficacy outcomes (response rates, progression-free survival, overall survival)
  • Safety profile and adverse events
  • Recommended dosing
  • Patient population characteristics
  • Comparison to standard therapies

To obtain accurate information about PF-06821497 phase 2 results, you would need to access the primary trial publications, conference presentations, or regulatory submissions specific to this investigational agent.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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