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cxcr1/2 inhibitor sx-682

Generic: CXCR1/2 Inhibitor SX-682

cxcr1/2 inhibitor sx-682: 5 clinical trials tracked.

cxcr1/2 inhibitor sx-682 evidence translation

What we can confirm

5 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about cxcr1/2 inhibitor sx-682, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence4 indications · 0 study sponsors
Clinical Trial Registry Records (5)

ASpiRE: A Proof-of-mechanism and Proof-of-concept Clinical Trial Evaluating the Safety, Tolerability, Biological and Anti-tumour Activity of Apalutamide With Dual CXCR1 and CXCR2 Blockade by SX-682 for Men Suffering From Metastatic Castration-resistant Prostate Cancer (mCRPC)

NCT07002320Registry updated 2026-09-08·Phase 1/Phase 2
Recruiting

Primary endpoint: Biologically active and tolerable dose range

Interventionalopen78 targetStarted 2025-04Completion 2029-104 sites · Switzerland, United KingdomInstitute of Cancer Research, United Kingdom

A Phase 2, Single-Arm Study of the CXCR1/2 Inhibitor SX-682 Plus Enzalutamide in Men With ARPI-Resistant Metastatic Castration Resistant Prostate Cancer, the SYNERGY-201 Trial

NCT06228053Registry updated 2025-12-22·Phase 2
Recruiting

Primary endpoint: Clinical Benefit

Interventionalopen53 targetStarted 2024-11Completion 2028-066 sites · United StatesSyntrix Biosystems, Inc.

An Open-label Phase 1 Study to Evaluate the Safety and Tolerability of SX-682 in Combination With Nivolumab as a Maintenance Therapy in Patients With Metastatic Pancreatic Ductal Adenocarcinoma

NCT04477343Registry updated 2026-07-06·Phase 1
Active, not recruiting

Primary endpoint: Maximum tolerable dose [Safety and Tolerability]

Interventionalopen20 targetStarted 2020-11Completion 2026-121 site · United StatesUniversity of Rochester

Phase Ib/II Trial of SX-682 in Combination With Nivolumab for Refractory RAS Mutated (RAS) Microsatellite Stable (MSS) Metastatic Colorectal Cancer (mCRC) (STOPTRAFFIC-1)

NCT04599140Registry updated 2026-07-20·Phase 1/Phase 2
Active, not recruiting

Primary endpoint: Incidence of adverse events (AEs)

Interventionalopen51 enrolledStarted 2020-10Completion 2026-071 site · United StatesM.D. Anderson Cancer Center

A Phase 1, Open-Label, Dose-Escalation With Expansion Study of SX-682 Alone and in Combination With Oral or Intravenous Decitabine in Subjects With Myelodysplastic Syndrome

NCT04245397Registry updated 2025-12-23·Phase 1
Recruiting

Primary endpoint: SX-682 Maximum Tolerated Dose (MTD)

Interventionalopen151 targetStarted 2020-06Completion 2029-037 sites · United StatesSyntrix Biosystems, Inc.