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NCT00790010
Bevacizumab Plus Ipilimumab in Patients With Unresectable Stage III or IV Melanoma
Phase 1 trial testing Bevacizumab Plus Ipilimumab Cohort 1 in Melanoma in 46 participants. Completed in 22 June 2018.
22 June 2018
Quick facts
| Lead sponsor | Dana-Farber Cancer Institute |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 46 |
| Start date | 26 February 2009 |
| Primary completion | 22 June 2018 |
| Estimated completion | 22 June 2018 |
| Sites | 3 locations across United States |
Drugs / interventions tested
- Bevacizumab Plus Ipilimumab Cohort 1 — full drug profile →
- Bevacizumab Plus Ipilimumab Cohort 2
- Bevacizumab Plus Ipilimumab Cohort 3
- Bevacizumab Plus Ipilimumab Cohort 4
Conditions studied
- Melanoma — all drugs for Melanoma →
Sponsor
Dana-Farber Cancer Institute
Who can join
18 and older, any sex, with Melanoma. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this research study is to determine the safety of using the study drugs bevacizumab and ipilimumab together, and the doses in combination which can be given to people safely. This study also seeks to investigate whether using both study drugs lengthens the amount of time before the participants melanoma worsens.
Publications & conference data
8 peer-reviewed publications reference this trial (live from Europe PMC):
-
Combining immunotherapy and targeted therapies in cancer treatment.
Vanneman M, Dranoff G. · · 2012 · cited 1134× · PMID 22437869 · DOI 10.1038/nrc3237 -
Synergistic effect of immune checkpoint blockade and anti-angiogenesis in cancer treatment.
Yi M, Jiao D, Qin S, Chu Q, et al · · 2019 · cited 487× · PMID 30925919 · DOI 10.1186/s12943-019-0974-6 -
Melanoma treatment in review.
Domingues B, Lopes JM, Soares P, Pópulo H. · · 2018 · cited 432× · PMID 29922629 · DOI 10.2147/itt.s134842 -
PD-1 as a potential target in cancer therapy.
McDermott DF, Atkins MB. · · 2013 · cited 309× · PMID 24403232 · DOI 10.1002/cam4.106 -
Soluble PD-L1 as a Biomarker in Malignant Melanoma Treated with Checkpoint Blockade.
Zhou J, Mahoney KM, Giobbie-Hurder A, Zhao F, et al · · 2017 · cited 291× · PMID 28522460 · DOI 10.1158/2326-6066.cir-16-0329 -
Targeting cytokine and chemokine signaling pathways for cancer therapy.
Yi M, Li T, Niu M, Zhang H, et al · · 2024 · cited 264× · PMID 39034318 · DOI 10.1038/s41392-024-01868-3 -
Anti-Angiogenic Therapy: Current Challenges and Future Perspectives.
Lopes-Coelho F, Martins F, Pereira SA, Serpa J. · · 2021 · cited 254× · PMID 33916438 · DOI 10.3390/ijms22073765 -
Control of the immune response by pro-angiogenic factors.
Voron T, Marcheteau E, Pernot S, Colussi O, et al · · 2014 · cited 252× · PMID 24765614 · DOI 10.3389/fonc.2014.00070
Verify or expand the search:
- PubMed search for NCT00790010
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT00790010 (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 Dana-Farber Cancer Institute
- Last refreshed: 11 May 2023
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/NCT00790010.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing