Safety Study for Beta Thalassemia Subjects on PTG-300

NCT04054921 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2021-07-16

No results posted yet for this study

Summary

In this study will investigate long term safety and use of the PTG-300 in Beta Thalassemia patients.

Conditions

  • β-thalassemia
  • Ineffective Erythropoiesis

Interventions

DRUG

PTG-300

PTG-300 is a hepcidin Mimetic

Sponsors & Collaborators

  • Protagonist Therapeutics, Inc.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
12 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-05-10
Primary Completion
2020-07-31
Completion
2020-07-31
FDA Drug
Yes

Countries

  • United States
  • Greece
  • Lebanon
  • Malaysia
  • Thailand
  • Tunisia
  • Turkey (Türkiye)
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04054921 on ClinicalTrials.gov