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NCT01636622
Study of Vemurafenib, Carboplatin, and Paclitaxel
Phase 1 trial testing Vemurafenib in Advanced Cancers in 21 participants. Completed in 21 April 2020.
21 April 2020
Quick facts
| Lead sponsor | M.D. Anderson Cancer Center |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 21 |
| Start date | 9 July 2012 |
| Primary completion | 21 April 2020 |
| Estimated completion | 21 April 2020 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Vemurafenib (vemurafenib) — full drug profile →
- Carboplatin (Carboplatin) — full drug profile →
- Paclitaxel — full drug profile →
Conditions studied
- Advanced Cancers — all drugs for Advanced Cancers →
Sponsor
M.D. Anderson Cancer Center — full company profile →
Who can join
12 and older, any sex, with Advanced Cancers. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this clinical research study is to find the highest tolerable dose of vemurafenib that can be given in combination with carboplatin and paclitaxel patients with advanced cancer. The safety of the study drug combination will also be studied. Vemurafenib is designed to block a protein (called mutated BRAF) that is only found in moles (spots) of the skin and certain types of cancer cells. This drug may slow the growth of or kill these cells. Carboplatin is designed to slow the growth of cancer cells by stopping them from making new DNA (the genetic material of cells). Paclitaxel is designed to slow the growth of cancer cells by stopping them from dividing into new cells.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
-
BRAF v600E-mutant cancers treated with vemurafenib alone or in combination with everolimus, sorafenib, or crizotinib or with paclitaxel and carboplatin (VEM-PLUS) study.
Nelson BE, Roszik J, Janku F, Hong DS, et al · · 2023 · cited 15× · PMID 36801912 · DOI 10.1038/s41698-022-00341-0 -
Phase 1 study of the combination of vemurafenib, carboplatin, and paclitaxel in patients with BRAF-mutated melanoma and other advanced malignancies.
Bhatty M, Kato S, Piha-Paul SA, Naing A, et al · · 2019 · cited 10× · PMID 30383888 · DOI 10.1002/cncr.31812 -
Genomics-Driven Precision Medicine in Pediatric Solid Tumors.
Suthapot P, Chiangjong W, Chaiyawat P, Choochuen P, et al · · 2023 · cited 7× · PMID 36900212 · DOI 10.3390/cancers15051418
Verify or expand the search:
- PubMed search for NCT01636622
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Vemurafenib
Trials testing the same drug.
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- NCT06440850 — Vemurafenib and Cobimetinib for the Treatment of Patients With High Risk Differentiated Thyroid Carcinoma With BRAFV600E · Phase 2 · recruiting
- NCT05238831 — SMMART Adaptive Clinical Treatment (ACT) Trial · EARLY_PHASE1 · withdrawn
- NCT05233332 — Study of HL-085 and Vemurafinib in Metastatic Colorectal Cancer (mCRC) · Phase 2 · unknown
Other recruiting trials for Advanced Cancers
Currently open trials in the same condition.
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- NCT03375983 — Plasmodium Immunotherapy for Advanced Cancers · Phase 1, PHASE2 · recruiting
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Other M.D. Anderson Cancer Center trials
Trials by the same sponsor.
- NCT07053020 — A Phase 1b/2 Open-label, Dose-ranging Safety and Efficacy Study of Oral Cladribine in Patients With Acute Myeloid Leukem · Phase 1, PHASE2 · not yet recruiting
- NCT07052994 — A Phase Ia/Ib Trial of Revumenib Combined With Cytarabine, Daunorubicin, and Gemtuzumab Ozogamicin (GO) in Frontline and · Phase 1 · not yet recruiting
- NCT07137481 — Phase II Study of CD5 CAR Engineered IL15-transduced Cord Blood-derived NK Cells in Conjunction With Lymphodepleting Che · Phase 2 · not yet recruiting
- NCT07162480 — Phase II Trial of Puxitatug Samrotecan (AZD8205) in Advanced, Recurrent or Metastatic (R/M) Aggressive Adenoid Cystic Ca · Phase 2 · not yet recruiting
- NCT07076498 — Engineered HSV-1 M032 for the Treatment of Children and Adults With Newly Diagnosed Diffuse Midline Glioma After Standar · Phase 1 · not yet 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 NCT01636622 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by M.D. Anderson Cancer Center
- Last refreshed: 18 June 2020
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/NCT01636622.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing