Last update 24 Feb 2026

NGM-707

Overview

Basic Info

Drug Type
Bispecific antibody
Synonyms
NGM 707, NGM707
Action
inhibitors
Mechanism
LILRB1 inhibitors(Leukocyte immunoglobulin-like receptor B1 inhibitors), LILRB2 inhibitors(Leukocyte immunoglobulin-like receptor subfamily B member 2 inhibitors), Immunologic cytotoxicity
Inactive Indication-
Originator Organization
Active Organization
Inactive Organization-
Drug Highest PhasePhase 2
First Approval Date-
Regulation-
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Metastatic Solid TumorPhase 2
United States
01 Sep 2023
Metastatic Solid TumorPhase 2
Canada
01 Sep 2023
Metastatic Solid TumorPhase 2
France
01 Sep 2023
Metastatic Solid TumorPhase 2
Israel
01 Sep 2023
Metastatic Solid TumorPhase 2
Italy
01 Sep 2023
Metastatic Solid TumorPhase 2
South Korea
01 Sep 2023
Metastatic Solid TumorPhase 2
Spain
01 Sep 2023
Metastatic Solid TumorPhase 2
Taiwan Province
01 Sep 2023
Solid tumorPhase 2
United States
01 Sep 2023
Solid tumorPhase 2
Canada
01 Sep 2023
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 1/2
82
NGM707 monotherapy
pjhymvknhy(oyjncgrbdw) = jvkjhncscx tftekpgcgj (bgdkiqmwej )
Positive
24 May 2024
NGM707 copembrolizumabembrolizumab
pjhymvknhy(oyjncgrbdw) = zymhgdwxeg tftekpgcgj (bgdkiqmwej )
Phase 1/2
46
ixewgjoxhe(odddzzmrpl) = owjsxapkme yzzcwfofcl (ybujdxaius )
Positive
05 Apr 2024
Phase 1/2
-
apvimjbbgl(jzqsgjunch) = Decreased protein expression of the immunosuppressive myeloid marker CD163 was observed following treatment in both blood and tumor for a subset of patients qjdjvkvcxg (bngcfitfah )
-
22 Mar 2024
Phase 1
37
wgnuomxdkp(bkldrodmes) = hetpvuxgti rdrztagizx (wceiaifuhn )
Positive
09 Jan 2024
wgnuomxdkp(bkldrodmes) = ptucuwqiys rdrztagizx (wceiaifuhn )
Phase 1
33
hnlebfxigb(iqgizmahfe) = rmzpymjcyp hbzticjemu (gplrmvzkss )
Positive
08 Dec 2022
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Clinical Trial

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Approval

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Biosimilar

Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.
Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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