Ozmosi | PR-600 Drug Profile
Drug Search Results
Using advanced filters...
Advanced Search [+]

PR-600

Alternative Names: pr-600, pr600
Clinical Status: Active
Latest Update: 2022-07-18
Latest Update Note: Clinical Trial Update

Product Description

Prometheus has selected a clinical candidate for PR600, targeting an undisclosed member of the tumor-necrosis factor superfamily for the treatment of IBD and is initiating IND-enabling studies. "Partnering with Dr. Falk on PR600 has enabled us to accelerate the PR600 program by sharing costs, resources, and drug development know-how, which has resulted in the achievement of this important milestone within the first year of our collaboration," said Mark McKenna, President and CEO of Prometheus. "We expect to file an Investigational New Drug Application for PR600 in the third quarter of 2022 and plan to explore its utility in other immune-mediated indications beyond IBD." (Sourced from: https://ir.prometheusbiosciences.com/news-releases/news-release-details/prometheus-biosciences-achieves-milestone-payment-dr-falk-pharma)

Mechanisms of Action: TNF Antagonist

Novel Mechanism: No

Modality: Antibody

Route of Administration: Intravenous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Merck
Company Location: Eastern America
Company CEO: Robert M. Davis
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 0: Colitis, Ulcerative|Crohn Disease

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated