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Pyxis Oncology

Pyxis Oncology is a clinical-stage company developing next-generation antibody-drug conjugates and immunotherapies for difficult-to-treat solid tumors. Its lead candidate, micvotabart pelidotin (MICVO, formerly PYX-201), is an antibody-drug conjugate that targets extradomain-B fibronectin, a structural component of the tumor extracellular matrix rather than a surface antigen on the cancer cell itself; it holds FDA Fast Track designation and is being evaluated in Phase 1 monotherapy cohorts and in a Phase 1/2 combination study with Merck's pembrolizumab, with recurrent and metastatic head and neck squamous cell carcinoma the focus indication. A portfolio prioritization narrowed development onto that lead program. Founded in 2018 as a spinout of Longwood Fund with an early licensing relationship with Pfizer, and headquartered in Boston, Massachusetts, the company went public on Nasdaq in October 2021. It remains pre-revenue and funds development from the balance sheet: on September 30, 2026 it priced a registered public offering of 36,047,919 common shares, or pre-funded warrants in lieu, paired with warrants for expected gross proceeds of approximately $110 million and up to $282.6 million if the accompanying warrants are exercised in full.

Company Info

Sector:Clinical-Stage Oncology / Antibody-Drug Conjugates
Headquarters:Boston, Massachusetts, USA
Founded:2018

Upcoming Milestones & Key Dates

October 2026
Corporate / Financing

Closing of the September 30, 2026 registered public offering (approximately $110 million expected gross proceeds; up to $282.6 million with warrants)

November 2026
Earnings

Third-quarter 2026 financial results

Clinical Development Pipeline

Micvotabart pelidotin (MICVO, formerly PYX-201)

Target: Extradomain-B fibronectin (extracellular-matrix ADC)
Recurrent/metastatic head and neck squamous cell carcinoma and other advanced solid tumors
Preclinical
Phase 1
Phase 2
Phase 3
Approved

PYX-201-102 combination study

Target: MICVO plus Merck's anti-PD-1 therapy KEYTRUDA (pembrolizumab)
Recurrent/metastatic head and neck squamous cell carcinoma and advanced solid tumors
Preclinical
Phase 1
Phase 2
Phase 3
Approved

Recent News

No recent news updates available for this company.

Leadership Team

Thomas Civik

Chief Executive Officer and Chairman of the Board

Nelson Azoulay, MS, MBA

Chief Business Officer

Careers & Job Openings

See all open roles

Multiple Departments
Boston, Massachusetts, USA
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