Summary

Eligibility
for people ages 18-83 (full criteria)
Location
at UCSF
Dates
study started
completion around

Description

Summary

TX000045-003 is a double-blind, randomized, parallel group, placebo-controlled, proof- of-concept (POC) study, evaluating 2 dose regimens of TX000045 over the course of a 24-week treatment period (the APEX study).

Official Title

A Phase 2, Double-blind, Randomized, Placebo-Controlled Study to Assess the Efficacy and Safety of TX000045 After 24 Weeks of Treatment in Patients With Pulmonary Hypertension Secondary to Heart Failure With Preserved Ejection Fraction (PH-HFpEF)

Details

This study will enroll approximately 180 participants and eligible patients will be randomized to one of 3 treatment arms:

  • Arm 1: Treatment Group 1: Placebo delivered subcutaneously (SC) every 2 weeks (Q2W) for 24 weeks
  • Arm 2: Treatment Group 2: TX000045 SC at Dose A Q2W for 24 weeks
  • Arm 3: Treatment Group 3: TX000045 SC at Dose B Q2W alternating with Placebo Q2W for 24 weeks

Keywords

Pulmonary Hypertension, Heart Failure With Preserved Ejection Fraction, Hypertension, Heart Failure, TX000045- Dose A, TX000045- Dose B

Eligibility

Locations

  • San Francisco not yet accepting patients
    San Francisco California 94143 United States
  • Scottsdale accepting new patients
    Scottsdale Arizona 85258 United States
  • Aurora accepting new patients
    Aurora Colorado 80045 United States

Details

Status
accepting new patients at some sites,
but this study is not currently recruiting here
Start Date
Completion Date
(estimated)
Sponsor
Tectonic Therapeutic
ID
NCT06616974
Phase
Phase 2 research study
Study Type
Interventional
Participants
Expecting 180 study participants
Last Updated