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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 developer

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 · 2 study sponsors
Clinical Trials (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)

NCT07002320·Phase 1/Phase 2·UTHR
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

NCT06228053·Phase 2·KYNB
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

NCT04477343·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)

NCT04599140·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

NCT04245397·Phase 1
Recruiting

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

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