Drugs / DALMITAMIG

Trials 5

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/21 trial
Phase 1/2 NCT04626635 Dec 2020 → Nov 2026 expected cancer Regeneron Pharmaceuticals Active not recruiting No outcome recorded
Phase 24 trials
Phase 2 NCT07281768 Jul 2026 → Jul 2030 expected colorectal cancer Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Recruiting No outcome recorded
Phase 2 NCT07058012 Apr 2026 → Apr 2029 expected colorectal cancer NSABP Foundation Inc Recruiting No outcome recorded
Phase 2 NCT07154290 Mar 2026 → Jun 2030 expected non-small cell lung carcinoma Regeneron Pharmaceuticals Recruiting No outcome recorded
Phase 2 NCT06465329 Nov 2024 → May 2027 expected non-small cell lung carcinoma Regeneron Pharmaceuticals Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2024-05-23 Regeneron Pharmaceuticals Results Promising Anti-tumor Activity of Novel Costimulatory Bispecific Antibody REGN7075 (EGFRxCD28) in Combination with Libtayo® (cemiplimab) to be Reported at ASCO regeneron.com ↗
Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced positive new results from an ongoing Phase 1/2 trial evaluating its first-in-class costimulatory bispecific antibody, REGN7075 (EGFRxCD28), in combination with Libtayo® (cemiplimab) in patients with advanced solid tumors.

All press releases naming this drug 1 release

DateIssuerRelease

Evidence & citations 8 cited values

Every value below carries the sentence it was read from. 6 sources stand behind the page.

FieldValueCited text
Known as DALMITAMIG ChEMBL registry synonym — accepted as the source's own label CHEMBL6068437 ↗
Known as Marlotamig ClinicalTrials.gov intervention name — accepted as the source's own label NCT07154290 ↗
Known as REGN7075 “Cemiplimab 350mg + REGN7075 2700mg intravenously” NCT07058012 ↗
3

NCT04626635 ↗

NCT06465329 ↗

NCT07281768 ↗

Modality Monoclonal antibody — CHEMBL6068437 ↗
Route Intravenous “Intravenous (IV) infusion or subcutaneous (SC) injection will be administered every week (QW) or every 3 weeks (Q3W)” NCT04626635 ↗
Route Subcutaneous “Intravenous (IV) infusion or subcutaneous (SC) injection will be administered every week (QW) or every 3 weeks (Q3W)” NCT04626635 ↗
Target CD28 “REGN7075 (EGFRxCD28 Costimulatory Bispecific Antibody)” NCT04626635 ↗
Target EGFR “REGN7075 (EGFRxCD28 Costimulatory Bispecific Antibody)” NCT04626635 ↗