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Study details
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A First-in-human, 3-part Study of MRT-8102 in Healthy Participants and Participants at Cardiovascular Risk With Elevated CRP

Monte Rosa Therapeutics, Inc
NCT IDNCT07119125ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

100

Study length

about 9 months

Ages

18–65

Locations

4 sites in FL, KS, MO +1

About this study

Researchers are testing a new drug called MRT-8102 to see if it's safe for people who are healthy or have heart problems. The trial will involve giving the drug or a placebo (inactive pill) in different ways over several weeks.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take MRT-8102
  • 2.Take Placebo
PhasePhase 1
Primary goalTo evaluate the safety and tolerability of 28-day daily dosing of MRT-8102 in participants at cardiovascular risk with elevated CRP

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low10%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Primary: To evaluate the safety and tolerability of 28-day daily dosing of MRT-8102 in participants at cardiovascular risk with elevated CRP, To evaluate the safety and tolerability of multiple ascending doses of MRT-8102 in healthy adult participants., To evaluate the safety and tolerability of single doses of MRT-8102 in healthy adult participants

Secondary: Assess the effect of a high-fat/high-calorie meal on the PK (peak plasma concentration) of MRT-8102 02 in healthy adult participants, Assess the effect of a high-fat/high-calorie meal on the PK (plasma concentration versus time) of MRT-8102 02 in healthy adult participants, Assess the impact of MRT-8102 on serum concentration of CRP, Characterize the PK Profile (peak plasma concentration) of MRT-8102 after single doses of MRT-8102 in healthy adult participants, Characterize the PK Profile (peak plasma concentration) of MRT-8102 when administered daily to participants at cardiovascular risk with elevated CRP, Characterize the PK Profile (plasma concentration versus time) of MRT-8102 after single doses of MRT-8102 in healthy adult participants, Characterize the PK Profile (plasma concentration versus time) of MRT-8102 when administered daily to participants at cardiovascular risk with elevated CRP, Characterize the PK profile (peak plasma concentration) of MRT-8102 in plasma after multiple doses of MRT-8102 in healthy adult participants