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Revelation Biosciences Selects Avance Clinical as CRO for Phase 2/3 TITAN Study

Key Takeaway: Revelation Biosciences has appointed Avance Clinical as the contract research organization for its Phase 2/3 TITAN study. This study will evaluate the efficacy of Gemini in treating patients with acute kidney injury (AKI). The partnership is expected to strengthen the clinical development process for this important therapy.

Market Sentiment Analysis

POSITIVE FACTORS

  • Revelation Biosciences is advancing its clinical research.
  • Collaboration with Avance Clinical enhances study capabilities.
  • The TITAN study aims to address a critical medical need.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Cash runway
~9 mo
Medium dilution risk
Lead asset
Gemini
Phase 1 · Renal Insufficiency, Chronic

Full Press Release Details

SAN DIEGO--(BUSINESS WIRE)---- $REVB #AKI--Revelation Biosciences, Inc. (NASDAQ: REVB) (the “Company” or “Revelation”), a clinical-stage life sciences company developing innovative solutions to treat acute and chronic disease, today announced that it has selected Avance Clinical, a full-service contract research organization (CRO) with global operations, to serve as the CRO for its Phase 2/3 adaptive-design TITAN study for evaluating Gemini in patients with acute kidney injury (AKI). The importance of hiring

Frequently Asked Questions

What is the TITAN study?

The TITAN study is a Phase 2/3 adaptive-design clinical trial evaluating Gemini for acute kidney injury.

Who is conducting the TITAN study?

Avance Clinical has been selected as the contract research organization for the TITAN study.

What condition does the TITAN study target?

The study targets acute kidney injury (AKI) in patients.

What is the role of Avance Clinical?

Avance Clinical will manage the clinical trial operations for the TITAN study.

Last updated: Aug 19, 2026