Actively Recruiting

Phase 1
Age: 18Years - 55Years
All Genders
Healthy Volunteers
NCT06049095

A Phase 1 Single and Multiple Ascending Dose Study of LTG-001 Administered Orally in Healthy Participants

Led by Latigo Biotherapeutics · Updated on 2026-01-23

204

Participants Needed

1

Research Sites

132 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a sequential, randomized, double-blind, placebo-controlled Phase 1 single (SAD) and multiple (MAD) ascending dose study to evaluate the safety, tolerability, and pharmacokinetics (PK) of orally or intravenously administered LTG-001 in healthy male and female participants

CONDITIONS

Official Title

A Phase 1 Single and Multiple Ascending Dose Study of LTG-001 Administered Orally in Healthy Participants

Who Can Participate

Age: 18Years - 55Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male and female participants aged 18 to 55 years, inclusive
  • Healthy with no significant medical abnormalities based on medical history, physical exams, lab tests, and ECG
  • Body mass index (BMI) between 18 and 32 kg/m2 inclusive
Not Eligible

You will not qualify if you...

  • Unable to take oral medications or have gastrointestinal problems affecting absorption
  • Significant cardiovascular, hematological, renal, hepatic, pulmonary, endocrine, gastrointestinal, immunological, dermatological, neurological, or psychiatric disease
  • History or current abuse of alcohol or recreational drugs
  • Donated more than 500 mL of blood within 3 months before study start
  • Known psychiatric disorders interfering with study cooperation
  • Under legal custodianship

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Clinical Research Unit

Christchurch, New Zealand

Actively Recruiting

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Research Team

D

Desmond Padhi

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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