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NCT00006089
Trastuzumab in Treating Patients With Stage III, Stage IV, or Recurrent Endometrial Cancer
Phase 2 trial testing Laboratory Biomarker Analysis in Endometrial Adenocarcinoma in 34 participants. Completed in 31 January 2010.
4 September 2007
Quick facts
| Lead sponsor | National Cancer Institute (NCI) |
|---|---|
| Phase | Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 34 |
| Start date | 18 September 2000 |
| Primary completion | 4 September 2007 |
| Estimated completion | 31 January 2010 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Laboratory Biomarker Analysis — full drug profile →
- Trastuzumab (trastuzumab) — full drug profile →
Conditions studied
- Endometrial Adenocarcinoma — all drugs for Endometrial Adenocarcinoma →
- ERBB2 Gene Amplification — all drugs for ERBB2 Gene Amplification →
- Recurrent Uterine Corpus Carcinoma — all drugs for Recurrent Uterine Corpus Carcinoma →
- Stage III Uterine Corpus Cancer AJCC v7 — all drugs for Stage III Uterine Corpus Cancer AJCC v7 →
Sponsor
National Cancer Institute (NCI)
Who can join
18 and older, female only, with Endometrial Adenocarcinoma or ERBB2 Gene Amplification. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Monoclonal antibodies such as trastuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Phase II trial to study the effectiveness of trastuzumab in treating patients who have stage III, stage IV, or recurrent endometrial cancer.
Publications & conference data
5 peer-reviewed publications reference this trial (live from Europe PMC):
-
Targeted therapies in gynecological cancers: a comprehensive review of clinical evidence.
Wang Q, Peng H, Qi X, Wu M, et al · · 2020 · cited 114× · PMID 32728057 · DOI 10.1038/s41392-020-0199-6 -
HER2 expression patterns in paired primary and metastatic endometrial cancer lesions.
Halle MK, Tangen IL, Berg HF, Hoivik EA, et al · · 2018 · cited 58× · PMID 29169184 · DOI 10.1038/bjc.2017.422 -
Pathogenesis and Clinical Management of Uterine Serous Carcinoma.
Zhang L, Kwan SY, Wong KK, Solaman PT, et al · · 2020 · cited 21× · PMID 32183290 · DOI 10.3390/cancers12030686 -
Targeting receptor tyrosine kinases in ovarian cancer: Genomic dysregulation, clinical evaluation of inhibitors, and potential for combinatorial therapies.
Wei Y, Erfani S, Schweer D, de Gouvea R, et al · · 2023 · cited 15× · PMID 36911068 · DOI 10.1016/j.omto.2023.02.006 -
Genomics of uterine malignancies and the potential of precision medicine.
Polidano J, Jarratt A, Scott CL, Barker HE. · · 2025 · PMID 41306899 · DOI 10.1177/17588359251387395
Verify or expand the search:
- PubMed search for NCT00006089
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other recruiting trials for Endometrial Adenocarcinoma
Currently open trials in the same condition.
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Other National Cancer Institute (NCI) trials
Trials by the same sponsor.
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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 NCT00006089 (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 National Cancer Institute (NCI)
- Last refreshed: 31 July 2019
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/NCT00006089.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing