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Completed Phase 1Phase 2 Interventional

An Open-label Study of Povetacicept in Participants With Autoimmune Cytopenias (RUBY-4)

ClinicalTrials.gov ID: NCT05757570

Public ClinicalTrials.gov record NCT05757570. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 10:49 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Open-Label Study to Assess the Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics of Povetacicept in Subjects With Autoimmune Cytopenias (RUBY-4)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this clinical study is to evaluate povetacicept in adults with autoimmune cytopenias of immune thrombocytopenia, autoimmune hemolytic anemia, and cold agglutinin disease to determine if povetacicept is safe and potentially beneficial in treating these diseases. During the study treatment period participants will receive povetacicept approximately every 4 weeks for 6 months, with the possibility of participating in a 6-month study treatment extension period.

Study identification

NCT ID
NCT05757570
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
30 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 3, 2023 (Actual)
Primary completion
Aug 12, 2026 (Actual)
Completion
Aug 12, 2026 (Actual)
Last update posted
Sep 14, 2026

2023 – 2026

United States locations

U.S. sites
15
U.S. states
8
U.S. cities
14
Facility City State ZIP Site status
Investigational Site (230) Los Angeles California 90033 —
Investigational Site (401) Washington D.C. District of Columbia 20007 —
Investigational Site (419) Cooper City Florida 33024 —
Investigational Site (425) Miami Florida 33143 —
Investigational Site (219) Iowa City Iowa 52242 —
Investigational Site (435) Columbia Maryland 21044 —
Investigational site (405) Lake Success New York 11042 —
Investigational Site (423) New Hyde Park New York 11040 —
Investigational Site (421) New York New York 10028 —
Investigational Site (404) New York New York 10065 —
Investigational Site (420) Shirley New York 11967 —
Investigational Site (422) The Bronx New York 10469 —
Investigational Site (414) Charlotte North Carolina 28204 —
Investigational Site (402) Greenville North Carolina 27834 —
Investigational Site (411) Seattle Washington 98109 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05757570, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 14, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05757570 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →