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NCT07071961

Regorafenib (Reg) and Lorigerlimab (Lor), RELO Regimen, in Treatment of High-risk Patients With Colorectal Cancer With Radiographic Occult Molecular Residual Disease After End of Established Definitive Therapy [ReLOAD Trial]

Suspended Phase 2 Last updated 17 February 2026
What this trial tests

Phase 2 trial testing Regorafenib (CT) in Colorectal Cancer in 16 participants. Suspended.

Timeline
11 February 2026
Primary endpoint
1 May 2027
1 May 2029

Quick facts

Lead sponsorM.D. Anderson Cancer Center
PhasePhase 2
StatusSuspended
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment16
Start date11 February 2026
Primary completion1 May 2027
Estimated completion1 May 2029
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

M.D. Anderson Cancer Center — full company profile →

Who can join

18 and older, any sex, with Colorectal Cancer or Regorafenib. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To learn about the effects of the drugs regorafenib and lorigerlimab on circulating tumor DNA (ctDNA) in patients with CRC and who have radiographic occult minimal residual disease (MRD) after completing standard-of-care therapy

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Colorectal Cancer

Currently open trials in the same condition.

Other M.D. Anderson Cancer Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07071961.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing