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NCT06630247
A Dose-escalation, Dose-finding, and Expansion Study of XL495 in Participants With Locally Advanced or Metastatic Solid Tumors
Phase 1 trial testing XL495 in Solid Cancers in 9 participants. Terminated before completion.
7 May 2025
Quick facts
| Lead sponsor | Exelixis |
|---|---|
| Phase | Phase 1 |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | sequential |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 9 |
| Start date | 17 October 2024 |
| Primary completion | 7 May 2025 |
| Estimated completion | 7 May 2025 |
| Sites | 10 locations across United States |
Drugs / interventions tested
- XL495 — full drug profile →
- ADC cytotoxic agents — full drug profile →
Conditions studied
- Solid Cancers — all drugs for Solid Cancers →
- Solid Tumor Cancer — all drugs for Solid Tumor Cancer →
- Solid Tumor Malignancy — all drugs for Solid Tumor Malignancy →
- Urothelial Cancer (Urinary Bladder, Ureters, or Renal Pelvis Cancer) — all drugs for Urothelial Cancer (Urinary Bladder, Ureters, or Renal Pelvis Cancer) →
Sponsor
Exelixis — full company profile →
Who can join
18 and older, any sex, with Solid Cancers or Solid Tumor Cancer. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this study is to obtain safety, tolerability, PK, and preliminary clinical antitumor activity for XL495 as a single agent and in combination with select cytotoxic agents in participants with locally advanced or metastatic tumors for whom life-prolonging therapies do not exist or available therapies are intolerable/no longer effective.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06630247
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Solid Cancers
Currently open trials in the same condition.
- NCT07170293 — Phase II Trial of Tunlametinib in Patients With NRAS Mutant Non-melanoma Refractory Solid Tumors · Phase 2 · recruiting
- NCT07479667 — An Antibody-armored Dendritic Cell in Patients With Solid Tumors · Phase 1 · recruiting
- NCT07371663 — An Phase Ib/II Clinical Trial of TCC1727 Combination Therapy in Advanced Solid Tumors · Phase 1, PHASE2 · recruiting
- NCT07167381 — xDRIVE for Florida-based Cancer Patients · NA · recruiting
- NCT07058948 — Spatially Fractionated Radiotherapy Combined With Immunotherapy for Advanced Solid Tumors · Phase 2 · recruiting
Other Exelixis trials
Trials by the same sponsor.
- NCT06545331 — Study of XB010 in Subjects With Solid Tumors · Phase 1 · recruiting
- NCT05932862 — A Phase 1 Study of XL309 (ISM3091) Alone and in Combination in Participants With Advanced Solid Tumors · Phase 1 · recruiting
- NCT06191796 — Study of Zanzalintinib (XL092) + AB521 and Zanzalintinib + AB521 + Nivolumab in Participants With Advanced Clear Cell Re · Phase 1 · terminated
- NCT05144347 — Study of XL114 in Subjects With Non-Hodgkin's Lymphoma · Phase 1 · terminated
- NCT05176483 — Study of Zanzalintinib in Combination With Immuno-Oncology Agents in Participants With Solid Tumors · Phase 1 · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06630247 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Exelixis
- Last refreshed: 25 June 2025
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/NCT06630247.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing