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NCT00006079
Eflornithine To Prevent Cervical Cancer in Patients With Cervical Intraepithelial Neoplasia
Phase 2 trial testing Eflornithine in Cervical Cancer in 150 participants. Completed in 27 April 2004.
27 April 2004
Quick facts
| Lead sponsor | M.D. Anderson Cancer Center |
|---|---|
| Phase | Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | single group |
| Masking | triple |
| Primary purpose | prevention |
| Enrollment | 150 |
| Start date | 19 June 1998 |
| Primary completion | 27 April 2004 |
| Estimated completion | 27 April 2004 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Eflornithine (EFLORNITHINE) — full drug profile →
- Placebo
Conditions studied
- Cervical Cancer — all drugs for Cervical Cancer →
- Precancerous Condition — all drugs for Precancerous Condition →
Sponsor
M.D. Anderson Cancer Center — full company profile →
Who can join
18 and older, female only, with Cervical Cancer or Precancerous Condition. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. The use of eflornithine may be an effective way to prevent the recurrence of or further development of cervical cancer. PURPOSE: Randomized phase II trial to determine the effectiveness of eflornithine in preventing cervical cancer in patients who have cervical intraepithelial neoplasia.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT00006079
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Trials testing the same drug.
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Other recruiting trials for Cervical Cancer
Currently open trials in the same condition.
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Other M.D. Anderson Cancer Center trials
Trials by the same sponsor.
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- 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 NCT00006079 (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 M.D. Anderson Cancer Center
- Last refreshed: 25 October 2018
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/NCT00006079.
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