ImmuneWalk Therapeutics Inc


Clinical-stage biotechnology company developing therapies for immune-inflammatory indications based on discovery of a myeloid-cell adhesion checkpoint that controls monocyte and neutrophil entry into inflamed tissues. The lead clinical-stage candidate is a monoclonal antibody therapeutic designed to prevent myeloid cell migration; a first-in-human Phase 1 trial (randomized, blinded, placebo-controlled SAD/MAD) is ongoing. Preclinical efficacy has been reported in models of multiple sclerosis, rheumatoid arthritis, inflammatory bowel disease and metabolic dysfunction-associated steatohepatitis.

Industries

biotechnology

Nr. of Employees

small (1-50)

ImmuneWalk Therapeutics Inc

Pearl River, New York, United States, North America


Patents

Motile sperm domain containing protein 2 and inflammation

US-12109264-B2

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Motile sperm domain containing protein 2 and cancer

US-11945875-B2

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Motile sperm domain containing protein 2 antibodies and methods of use thereof

US-11697682-B2

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Products

Clinical-stage monoclonal antibody therapeutic targeting a myeloid adhesion checkpoint

A clinical-stage monoclonal antibody candidate engineered to inhibit a myeloid-cell adhesion checkpoint and prevent monocyte and neutrophil entry into inflamed tissues; being evaluated in a first-in-human Phase 1 SAD/MAD trial with PK/PD and biomarker endpoints.

IW-601

IW-601 is a subcutaneous immunomodulator evaluated in the POINTGUARD first-in-human clinical trial for safety, tolerability, pharmacokinetics, and pharmacodynamics.

Expertise Areas

  • Clinical trial management (early-phase SAD/MAD)
  • Myeloid-targeted immunology
  • Monoclonal antibody therapeutic development
  • Preclinical disease modeling for inflammatory indications
  • Show More (3)

Key Technologies

  • Monoclonal antibody therapeutics
  • Myeloid cell adhesion checkpoint targeting
  • β2-integrin modulation mechanism
  • Preclinical animal disease models (MS, RA, IBD, NASH/MASH)
  • Show More (2)

News & Updates

The Phase 1 Single Ascending Dose stage of the first-in-human trial met safety, tolerability, PK and PD endpoints.

Announcement of $7 million seed financing for the company.

Company presented therapeutic candidate data at industry events including a 2025 BIO convention presentation and other conference posters.

Company CEO scheduled to present at industry events (e.g., Longwood MIT CEO 2025).


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