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NCT05259189

A Study of NBL-012 in Healthy Chinese Subjects

Completed Phase 1 Last updated 20 July 2022
What this trial tests

Phase 1 trial testing NBL-012 Injection in Healthy Subjects in 52 participants. Completed in 23 May 2022.

Timeline
1 July 2021
Primary endpoint
23 May 2022
23 May 2022

Quick facts

Lead sponsorNovaRock Biotherapeutics, Ltd
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingdouble
Primary purposetreatment
Enrollment52
Start date1 July 2021
Primary completion23 May 2022
Estimated completion23 May 2022
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

NovaRock Biotherapeutics, Ltd — full company profile →

Who can join

Adults 18 to 45, any sex, with Healthy Subjects. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a phase 1, randomized, double-blind, placebo-controlled, sequential cohort study to evaluate the safety, tolerability and pharmacokinetics (PK) of NBL-012 as single ascending doses (SAD) administered subcutaneously to healthy Chinese subjects.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05259189.

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