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Completed Phase 2 Interventional Results available

CM-101 in PSC Patients -The SPRING Study

ClinicalTrials.gov ID: NCT04595825

Public ClinicalTrials.gov record NCT04595825. 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 Sep 4, 2026, 11:12 AM EDT

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

Official title

A Phase 2a, Randomized, Double-Blind, Placebo-Controlled, Clinical Trial Evaluating the Safety and Efficacy of CM-101 in Subjects With Primary Sclerosing Cholangitis (The SPRING Study)

Brief summary

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

This study is designed to assess the safety, tolerability and activity of the anti-human CCL24 monoclonal antibody CM-101 in adult subjects with Primary Sclerosing Cholangitis (PSC). At least 68 subjects at approximately 50 sites will be randomized to receive either CM-101 at doses of 10 mg/kg or 20 mg/kg or matching placebo.

Study identification

NCT ID
NCT04595825
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
ChemomAb Ltd.
Industry
Enrollment
77 participants

Conditions and interventions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Sep 30, 2020
Primary completion
Jan 9, 2025
Completion
Jan 9, 2025
Last update posted
Jul 1, 2026

2020 – 2025

United States locations

U.S. sites
8
U.S. states
6
U.S. cities
7
Facility City State ZIP Site status
Scripps Clinic Torrey Pines - site P83 La Jolla California 92037
UC Davis Health System - Midtown Ambulatory Care Center - site P79 Sacramento California 95816-5202
Northwestern University - site P77 Chicago Illinois 60611
Massachusetts General Hospital - site P95 Boston Massachusetts 02114
Harvard Medical School - Beth Israel Deaconess Medical Center (BIDMC) - Liver Center - site P81 Boston Massachusetts 02215
Gastro One - GI Diagnostic and Therapeutic Endoscopy Center - 1310 Wolf Park - site P82 Germantown Tennessee 38138-1741
Methodist Dallas Medical Center - site P72 Dallas Texas 75203
Virginia Commonwealth - site P94 Richmond Virginia 23284

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 25 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04595825, 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 Jul 1, 2026 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04595825 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →