NCT07620574 · Exelixis
Not yet recruiting
Enrolling by invitation
Company identity has not yet been verified
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Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.
NCT07620574 · Exelixis
Not yet recruiting
Enrolling by invitation
NCT05678673 · Exelixis
2025-07
2026-12-15
NCT05425940 · Exelixis
2026-05
2026-06-16
NCT05425940 · Exelixis
Estimated
Actual
NCT06943755 · Exelixis
2029-06
2029-06-30
NCT07428616 · Exelixis
Not yet recruiting
Recruiting
NCT07428616 · Exelixis
2028-02
2028-02-29
NCT01068782 · Exelixis
Completed
Terminated
NCT01068782 · Exelixis
measure: In the Randomized Phase, to evaluate the preliminary efficacy and tolerability of multiple regimens of XL184; measure: In the Expansion Phase, to evaluate the efficacy of XL184 treatment
measure: Randomized Phase: Number of Participants With Treatment Emergent Adverse Events (TEAEs); measure: Expansion Phase: Objective Response Rate (ORR)
NCT01995058 · Exelixis
measure: Radiographic progression free survival (PFS)
measure: Radiographic Progression Free Survival (PFS)
NCT03755791 · Exelixis
2021-03-08
2021-11-30
NCT04446117 · Exelixis
measure: Duration of Progression Free Survival per Response Evaluable Criteria in Solid Tumors version 1.1 (RECIST 1.1); measure: Duration of Overall Survival (OS)
measure: Duration of Progression Free Survival (PFS) Per Response Evaluable Criteria in Solid Tumors Version 1.1 (RECIST 1.1) by Blinded Independent Radiology Committee (BIRC); measure: Duration of Overall Survival (OS)
NCT03755791 · Exelixis
measure: Duration of Progression Free Survival (PFS) for the experimental arm vs. the control arm; measure: Duration of Overall Survival (OS) for the experimental arm vs. the control arm
measure: Progression Free Survival (PFS) for the Experimental Arm Versus the Control Arm in the PFS Intent to Treat (PITT) Population; measure: Overall Survival (OS) for the Experimental Arm Versus the Control Arm in the ITT Population
NCT05425940 · Exelixis
2025-08
2026-05
NCT05425940 · Exelixis
count: 874; type: ESTIMATED
count: 901; type: ACTUAL
NCT05425940 · Exelixis
Estimated
Actual
NCT05425940 · Exelixis
measure: Overall Survival
measure: Overall Survival (OS) of XL092 + Atezolizumab Versus Regorafenib in All Randomized Participants; measure: Overall Survival (OS) of XL092 + Atezolizumab Versus Regorafenib in Randomized Non-Liver Metastases (NLM) Participants