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NCT00801177
Phase I Study of the Fully Human Anti-Epidermal Growth Factor Receptor (EGFR) Monoclonal Antibody IMC-11F8 in Patients With Solid Tumors Who Have Failed Standard Therapy
Phase 1 trial testing IMC-11F8 in Solid Tumors in 60 participants. Completed in 1 February 2007.
1 February 2007
Quick facts
| Lead sponsor | Eli Lilly and Company |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | parallel |
| Masking | none |
| Enrollment | 60 |
| Start date | 1 November 2004 |
| Primary completion | 1 February 2007 |
| Estimated completion | 1 February 2007 |
| Sites | 2 locations across Netherlands |
Drugs / interventions tested
- IMC-11F8 — full drug profile →
- IMC-11F8 — full drug profile →
- IMC-11F8 — full drug profile →
- IMC-11F8 I.V. — full drug profile →
- IMC-11F8 — full drug profile →
- IMC-11F8 — full drug profile →
- IMC-11F8 — full drug profile →
- IMC-11F8 — full drug profile →
- IMC-11F8 — full drug profile →
- IMC-11F8 — full drug profile →
- IMC-11F8 — full drug profile →
- IMC-11F8 — full drug profile →
Conditions studied
- Solid Tumors — all drugs for Solid Tumors →
Sponsor
Eli Lilly and Company — full company profile →
Who can join
18 and older, any sex, with Solid Tumors. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Number of Participants with Adverse Events
Time frame: Approximately 24 Months -
Maximum Tolerated Dose of IMC-11F8
Time frame: Approximately 24 Months
Sponsor's own description
The purpose of this study is to determine if IMC-11F8 is safe for patients, and also to determine the best dose of IMC-11F8 to give to patients.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Antibody phage display libraries: contributions to oncology.
Dantas-Barbosa C, De Macedo Brigido M, Maranhao AQ. · · 2012 · cited 27× · PMID 22754305 · DOI 10.3390/ijms13055420 -
EGFR Monoclonal Antibodies in the Treatment of Squamous Cell Carcinoma of the Head and Neck: A View beyond Cetuximab.
Kono SA, Haigentz M, Yom SS, Saba N. · · 2012 · cited 4× · PMID 23056941 · DOI 10.1155/2012/901320
Verify or expand the search:
- PubMed search for NCT00801177
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Solid Tumors
Currently open trials in the same condition.
- NCT07529002 — Clinical Application of 89Zr-s-C1 PET/CT Imaging in Solid Tumors · recruiting
- NCT07416123 — A Study of GEN1106 in Participants With Solid Tumors · Phase 1 · recruiting
- NCT07522073 — A Study to Evaluate Chemotherapy With or Without INCB161734 in Previously Untreated, KRAS G12D-Mutated Metastatic Pancre · Phase 3 · recruiting
- NCT07395258 — A Study to Test Different Doses of BI 3923948 Alone and in Combination With an Anti-PD-1 Antibody in People With Differe · Phase 1 · recruiting
- NCT07505069 — Exploring the Clinical Value of RT01-89Zr PET Imaging in Solid Tumors · EARLY_PHASE1 · recruiting
Other Eli Lilly and Company trials
Trials by the same sponsor.
- NCT07533006 — A Study of LY4005130 in Adult Participants With Severe Alopecia Areata (Hair Loss) · Phase 2 · not yet recruiting
- NCT07533019 — A Study of LY4005130 in Adult Participants With Non-Segmental Vitiligo · Phase 2 · not yet recruiting
- NCT07247357 — A Study of LY4064809 in Healthy Adult Chinese Participants · Phase 1 · completed
- NCT07124013 — A Study of Olomorasib (LY3537982) in Healthy Japanese Participants · Phase 1 · completed
- NCT07030127 — A Study of LY3985863 in Healthy Participants · Phase 1 · completed
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 NCT00801177 (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 Eli Lilly and Company
- Last refreshed: 11 October 2010
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/NCT00801177.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing