necitumumab
necitumumab: sourced relationships with 1 company · 1 clinical trial tracked · 1 FDA decision.
necitumumab evidence translation
What we can confirm
1 FDA record · 1 tracked trial
What it means
What to watch
Prepared research question
How could necitumumab → LLY affect its developer, and what evidence supports the link?
Traceable citations · Unknowns marked
Dated Pipeline Records (1)
| Company | Dated record stage |
|---|---|
| ELI LILLY & Co (LLY) Reported 2015-11-24 · Current development: unknownSource | Approved |
Clinical Trial Registry Records (1)
UCLA L-08: A Phase Ib/II Study of Combined HER Inhibition Adding Necitumumab and Trastuzumab to Osimertinib in Patients With Refractory EGFR-Mutated Lung Cancer
Primary endpoint: Identification of the recommended phase II dose (R2PD) regimen for combination osimertinib, necitumumab, trastuzumab (ONT) therapy (Phase Ib)
FDA Decisions1 records
Frequently asked questions
Which companies have sourced relationships with necitumumab?
necitumumab has dated SEC/FDA relationship records for ELI LILLY & Co.
How many clinical trials involve necitumumab?
BioSniper tracks 1 clinical trial involving necitumumab.
What is necitumumab's latest FDA decision?
The most recent tracked FDA decision for necitumumab is Approval for 1 INDICATIONS AND USAGE PORTRAZZA™ is an epidermal growth factor receptor (EGFR) antagonist indicated, in combination with gemcitabine and cisplatin, for first-line treatment of patients with metastatic squamous non-small cell lung cancer. ( 1.1 ) Limitation of Use: PORTRAZZA is not indicated for treatment of non-squamous non-small cell lung cancer. ( 1.2 , 5.6 , 14.2 ) 1.1 Squamous Non-Small Cell Lung Cancer (NSCLC) PORTRAZZA™ is indicated, in combination with gemcitabine and cisplatin, for fir, dated November 24, 2015.