CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 20 target
Drug / intervention
nicotinamide adenine dinucleotid/nicotinamide mononucleotidedrug
Likely dose
nicotinamide adenine dinucleotid/nicotinamide mononucleotide 100mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06776510
NCT06776510Phase 2RecruitingUpdate OverdueUpdated 10mo ago · Completion was 6mo ago
Enrollment Stalled
Update Overdue

A Prospective, One-arm and Open Clinical Study to Assess Safety and Efficacy of Nicotinamide Adenine Dinucleotide in the Treatment of Primary Immune Thrombocytopenia

Institute of Hematology & Blood Diseases Hospital, China·interventional·Posted Jan 15, 2025·Updated Aug 5, 2025

In Brief

A Phase 2 clinical trial evaluating nicotinamide adenine dinucleotid/nicotinamide mononucleotide for Immune Thrombocytopenia and Treatment. Currently recruiting, targeting 20 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

To evaluate the safety and efficacy of nicotinamide adenine dinucleotide in the treatment of immune thrombocytopenia in patients who have not responded adequately or relapsed after first-line treatment and at least one second-line therapy including Anti-CD20 Antibody and/or TPO-RA.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 2RecruitingOverdue
20252026
First PostedJan 15, 2025
Enrollment StartJan 15, 2025
Primary CompletionDec 1, 2025
Study CompletionMar 1, 2026
TodayJul 1, 2026
Enrollment to primary: 11 monthsPosted 1.5 years ago

Interventions

nicotinamide adenine dinucleotid/nicotinamide mononucleotidedrug

Drug: intravenous nicotinamide adenine dinucleotide (Coenzyme I for Injection) administration This study adopts a prospective, single arm, open design method. Twenty subjects were enrolled in the study and were treated with nicotinamide adenine dinucleotide (100mg/d) for 1 week. Drug: oral nicotinamide mononucleotide administration This study adopts a prospective, single arm, open design method. Twenty subjects were enrolled in the study and were treated with nicotinamide mononucleotide 450mg BID for 2 weeks. The first stage is the main research stage (d0-w2), which is the core treatment period. The aim is to observe the safety and efficacy during treatment. The second stage (w2-w8) is the stage of withdrawal from the visit, mainly to observe the safety and continuous efficacy after treatment.