Salarius Pharmaceuticals Announces Patient Enrollment to Resume in Investigator-initiated Phase 1/2 Clinical Trial Using Seclidemstat with Azacitidine to Treat Hematologic Cancers

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Salarius Pharmaceuticals, Inc.
Salarius Pharmaceuticals, Inc.

HOUSTON, Feb. 03, 2025 (GLOBE NEWSWIRE) -- Salarius Pharmaceuticals, Inc. (Nasdaq: SLRX) announces that patient enrollment will resume in the investigator-initiated Phase 1/2 clinical trial evaluating seclidemstat in combination with azacitidine for the treatment of myelodysplastic syndrome (MDS) and chronic myelomonocytic leukemia (CMML). The trial is being conducted at the University of Texas MD Anderson Cancer Center (MDACC) and is listed as recruiting on clinical trials.gov – trial NCT04734990.

Seclidemstat is a novel oral reversible inhibitor of the LSD1 enzyme. Inhibiting LSD1 in preclinical in vivo hematologic models has previously demonstrated reprogramed cancer cell differentiation, reduced tumor burden and prolonged survival of treated animals studied.

As previously announced at the June 2024 European Hematology Association Annual Meeting, researchers at MDACC reported interim clinical trial results from this trial including a 43% overall response rate among 14 predominantly higher-risk MDS and CMML patients who previously failed or relapsed after hypomethylating agent therapy. In addition, researchers reported median overall survival of 18.5 months (95% CI, range 6.1-30.9 months) with median event-free survival of 7.2 months (95% CI, range 6.3-8.2 months). As reported, overall survival after failing therapy with hypomethylating agents is typically four to six months.

In July 2024 the U.S. Food and Drug Administration (FDA) placed the MDACC investigator-initiated trial under a partial clinical hold following a serious and unexpected adverse event. MDACC has addressed the FDA’s questions, and the partial clinical hold has been lifted.

“Coming off partial clinical hold is welcome news for Salarius stakeholders and for patients with advanced MDS and CMML, and we are excited for MDACC to enroll additional patients and build upon seclidemstat’s growing clinical database,” said David Arthur, President and CEO of Salarius Pharmaceuticals.

As announced on January 13, 2025, Salarius signed a definitive agreement under which Decoy Therapeutics, Inc. will merge with a wholly owned subsidiary of Salarius Pharmaceuticals, subject to certain closing conditions in the agreement. The newly formed company will be named Decoy Therapeutics. The proposed transaction is expected to facilitate multiple value-creating inflection points with Decoy’s pipeline of peptide conjugate therapeutics engineered by its IMP3ACT™ platform, which allows for the rapid computational design and manufacturing of innovative peptide conjugate therapeutics including rapid response to novel viral pathogens such as avian H5N1 flu. Decoy’s product pipeline targets unmet needs in respiratory infectious diseases and gastroenterology (GI) oncology indications.