Startup profile for TriGemX Bio: latest funding, latest known valuation, total disclosed funding, investors, status, sources, and why the company is interesting. Part of the Venture Capital Tracker startup directory.

Startup profile · funding coverage

TriGemX Bio funding, valuation and investors

Late-stage migraine biotech developing elismetrep, an oral TRPM8 channel blocker.

Keep track of TriGemX Bio

Save this profile to your VCT watchlist for a quick return.

View watchlist

Funding, valuation & investors

Answer-first snapshot

Latest funding

Financing (stage undisclosed)

$94M · October 1, 2026

Latest known valuation

Not publicly disclosed

Total disclosed equity funding

$94M

Excludes debt, grants, acquisitions, secondaries, and IPO proceeds.

Current status

private

growth · New York, New York

Investors in latest funding

Lead: The Column Group , TCGX , Viking Global Investors

Sources: latest funding Last verified: 2026-10-05T07:15:00Z

Overview

TriGemX Bio, formerly Kallyope, is a New York biotechnology company advancing elismetrep for the acute treatment of migraine. Elismetrep is an investigational oral blocker of the TRPM8 ion channel and is in Phase 3 trials.

Why TriGemX Bio is interesting

The $94 million financing funds an active pivotal program rather than early discovery. TriGemX is testing a mechanistically distinct migraine target after a positive Phase 2b study, with first Phase 3 results expected in mid-2027. The central risk is binary clinical and regulatory execution: elismetrep remains investigational and has not been approved.

Product & use cases

Elismetrep (K-304), a liquid-filled soft-gel formulation of an oral TRPM8 channel blocker for acute migraine treatment.

  • Acute treatment of migraine in adults.

Key facts

  • Closed $94 million of financing co-led by The Column Group, TCGX and Viking Global Investors.
  • Two pivotal studies and a long-term safety study form the Phase 3 program.
  • Relaunched from Kallyope as TriGemX Bio with a focused migraine strategy and new leadership.

Funding history (newest first)

Investors in our directory

Funds linked from TriGemX Bio's profile — open a fund page for stage focus and related deal articles.

Competitive landscape

Edge: A potentially first-in-class oral TRPM8 blocker with Phase 2b evidence and an active pivotal program.

TriGemX will compete for use in a migraine market transformed by CGRP-targeted drugs from AbbVie, Pfizer and Eli Lilly, alongside triptans and other acute therapies. Its argument is mechanistic differentiation through TRPM8 blockade. Commercial value will depend on Phase 3 efficacy, safety, onset and tolerability relative to established oral options.

  • AbbVie (Ubrelvy) incumbent

    Established oral CGRP antagonist for acute migraine treatment.

  • Pfizer (Nurtec ODT) incumbent

    Oral CGRP antagonist used for acute treatment and prevention.

  • Eli Lilly (Reyvow) alternative

    Non-CGRP oral acute migraine treatment with a distinct mechanism.

  • Triptans alternative

    Long-established acute migraine therapies used broadly as generics and brands.

Industries

Market / IPO context

Editorial / static context — not a live quote.

Related funding articles

Venture Capital Tracker pieces that cover TriGemX Bio's financing or category context.

FAQs about TriGemX Bio

Practical answers founders, operators, and investors typically search for.

TriGemX Bio closed a $94 million financing announced on October 1, 2026. The formal venture stage was not disclosed.
The Column Group, TCGX and Viking Global Investors co-led the financing.
Elismetrep, also known as K-304, is an investigational oral TRPM8 channel blocker being studied for acute migraine treatment.
TriGemX expects initial results from its first Phase 3 trial in mid-2027.
No. Elismetrep remains investigational and has not been approved by the FDA or another regulatory agency.

By Venture Capital Tracker

Last updated:

Editorial note: AI tools assisted with research, structure, or drafting. Venture Capital Tracker retains human editorial responsibility for factual accuracy, relevance, and source quality before publication.