Drugs / MRT-8102
last change Jul 2026 re-read 3 minutes ago

MRT-8102

Investigated by
Monte Rosa Therapeutics, Inc

Trials 1

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT07119125 Jun 2025 → Jul 2026 overdue — Monte Rosa Therapeutics, Inc Active not recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2026-03-17 Monte Rosa Therapeutics, Inc Results Monte Rosa Therapeutics Announces Fourth Quarter and Full-Year 2025 Financial Results and Business Updates monterosatx.com ↗
Newly announced unblinded safety data from MRT-8102 SAD/MAD cohorts continue to support favorable safety/tolerability profile and wide therapeutic window
2026-01-07 Monte Rosa Therapeutics, Inc Results Monte Rosa Therapeutics Announces Positive Interim Phase 1 Data of MRT-8102 Demonstrating Profound CRP Reductions in Elevated CVD-risk Subjects monterosatx.com ↗
After four weeks of MRT-8102 treatment, C-reactive protein (CRP) levels were reduced by 85%, and 94% of study participants achieved CRP values below 2 mg/L, a threshold associated with reduced cardiovascular disease (CVD) risk

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as MRT-8102 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07119125 ↗
Route Oral “when MRT-8102 is administered orally as single and multiple doses” NCT07119125 ↗