Drugs / Patritumab

Trials 9

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 14 trials
Phase 1 NCT02350712 Dec 2014 → Mar 2016 head and neck squamous cell carcinoma Daiichi Sankyo Completed No outcome recorded
Phase 1 NCT01957280 Jun → Oct 2013 cancer Daiichi Sankyo Completed No outcome recorded
Phase 1 NCT01479023 Apr 2012 → Jan 2013 carcinoma, lymphoma, sarcoma Washington University School of Medicine Terminated No outcome recorded
Phase 1 NCT00730470 Aug 2008 → Jul 2010 cancer U3 Pharma GmbH Completed No outcome recorded
Phase 1/22 trials
Phase 1/2 NCT01512199 Nov 2011 → Jan 2015 breast cancer Daiichi Sankyo Terminated No outcome recorded Stop: Business
Phase 1/2 NCT01211483 Sep 2010 → Oct 2013 non-small cell lung carcinoma Daiichi Sankyo Completed Mixed
Phase 22 trials · 1 missed
Phase 2 NCT02633800 Dec 2015 → Jan 2018 head and neck neoplasm Daiichi Sankyo Terminated Missed primary
Phase 2 NCT01042379 Mar 2010 → Dec 2030 expected HER2 positive breast carcinoma, angiosarcoma, female breast carcinoma, hormone receptor-positive breast cancer +1 QuantumLeap Healthcare Collaborative Recruiting No outcome recorded
Phase 31 trial
Phase 3 NCT02134015 Mar 2014 → Nov 2016 non-small cell lung carcinoma Daiichi Sankyo Terminated No outcome recorded

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2016-05-31 Daiichi Sankyo Results Daiichi Sankyo Provides Update on HER3-Lung Study of Patritumab in Non-Small Cell Lung Cancer (NSCLC) daiichisankyo.com ↗
Daiichi Sankyo Company, Limited (hereafter, Daiichi Sankyo) today announced that the two-part phase 3 HER3-Lung study of patritumab will not proceed into the second part.

Evidence & citations 7 cited values

Every value below carries the sentence it was read from. 10 sources stand behind the page.

FieldValueCited text
Known as patritumab “The purpose of this study was to evaluate the safety, dosimetry, and apparent receptor occupancy (RO) of [(64)Cu]DOTA-patritumab, a radiolabeled monoclonal antibody directed...” PMID 26567113 ↗ Jun 2016
5

NCT01957280 ↗

NCT02350712 ↗

NCT02633800 ↗

NCT01042379 ↗

NCT02134015 ↗

Known as AMG 888 “Randomized, Placebo Controlled, Double Blind Phase 1b/2 Study of U3-1287 (AMG 888) in Combination With Trastuzumab Plus Paclitaxel in Newly Diagnosed HER2 Positive Metastatic...” NCT01512199 ↗
Known as U3-1287 ClinicalTrials.gov intervention name — accepted as the source's own label NCT01512199 ↗
2

NCT01211483 ↗

NCT00730470 ↗

Action Inhibit “patritumab blocks HER3 activation” PMID 31648099 ↗ Oct 2019
Modality Monoclonal antibody “fully human monoclonal antibody” NCT00730470 ↗
Route Intravenous “IV Infusion” NCT00730470 ↗
Target ERBB3 “a radiolabeled monoclonal antibody directed against HER3/ERBB3” PMID 26567113 ↗ Jun 2016