Drug intelligence / Profile preview

NG-641

Development stage
Phase 1
Lead developer
Akamis Bio
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Gene Silencing → Gene Therapies, Oncolytic Viruses → Oncolytic Therapeutics, Gene Editing → Gene Therapies, Gene Addition/Replacement → Gene Therapies
Administration
Intravenous, Intratumoral
01

Overview

NG-641 is an experimental oncolytic adenoviral vector engineered to selectively infect and replicate in tumor cells. It encodes four immunostimulatory transgenes: a fibroblast activation protein (FAP)-directed bispecific T-cell activator antibody (FAP-TAc), interferon alpha (IFNα), and the chemokines CXCL9 and CXCL10. The FAP-targeted bispecific antibody redirects T cells to attack cancer-associated fibroblasts within the tumor microenvironment, while IFNα and the chemokines enhance immune cell recruitment and activation. This multi-pronged approach aims to remodel the tumor microenvironment for improved anti-tumor immunity. Developed by Akamis Bio (formerly PsiOxus Therapeutics), NG-641 is being investigated primarily for solid tumors including squamous cell carcinoma of the head and neck in early-phase clinical trials[1][2][3][4][5][6][7][8].

Other names
enadenotucirev-expressing FAP/CD3 bispecific FAP-TAc NG-641
02

Targets

FAP (Fibroblast activation protein alpha)CCR3 (C-C chemokine receptor type 3)IFNAR (Immune system modulation via type I interferon receptor)CD3 (T-cell surface glycoprotein CD3)

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