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Completed

NCT Number: NCT02452996

Safety Study of GNbAC1 Monoclonal Antibody in Healthy Male Volunteers

In this clinical study, the safety and tolerability of GNbAC1 as a treatment for MS patients will be evaluated in healthy male volunteers.

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Key information

Age range

18 year–55 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

PAREXEL Early Phase Clinical Unit

Berlin, 14050, Germany

About this study

The monoclonal antibody, GNbAC1, targets the envelope protein (Env) of the human endogenous retrovirus (HERV), also called multiple sclerosis associated retrovirus (MSRV), which is considered as a critical factor in the development of multiple sclerosis.

This study will assess the pharmacokinetics, safety and tolerability of GNbAC1 following single ascending doses (6, 18, and 36 mg/kg) administered via IV infusion.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy male subjects as determined by past medical history, physical examination, vital signs, ECG and laboratory tests at Screening and confirmed at Day -1 who have signed the informed consent.
  • Aged from 18 to 55 years, both inclusive.

Exclusion criteria

  • History of serious adverse reactions or hypersensitivity to any drug.
  • Presence or history of any allergy requiring acute or chronic treatment (seasonal allergic rhinitis that requires no treatment may be tolerated).
  • Need of any prescription medication within 15 days prior to the administration of the study drug and/or non-prescription medication within 7 days prior to the administration of the study drug or anticipated need for any concomitant medication during the study.
  • Participation in a clinical trial during the previous 3 months, i.e. from completion of the previous trial to the planned first administration of the current trial.

NOTE: Other protocol-defined Inclusion/Exclusion criteria may apply.

Treatment and study plan

GNbAC1

Drug

Single dose of IMP, IV infusion

Primary outcomes

  1. safety and tolerability of single ascending doses of GNbAC1 in healthy male subjects

    Time frame: 57 days

    AE, SAE, vital signs, ECG, clinical laboratory values

Secondary outcomes

  1. PK characteristics: GNbAC1 serum concentrations

    Time frame: 57 days

    GNbAC1 serum concentrations over time

  2. immunogenicity in terms of antibodies against GNbAC1 (anti-drug antibodies)

    Time frame: 57 days

    antibodies against GNbAC1 (anti-drug antibodies)

  3. ratio of serum to CSF GNbAC1 concentration

    Time frame: 29 days

    GNbAC1 cerebrospinal fluid concentration at Day 2 and Weeks 2 and 4 after administration

Sponsors and collaborators

Lead sponsor

GeNeuro Innovation SAS

Industry

Registry information

Official study title

A Randomised, Double-Blind, Placebo Controlled, Single Ascending Doses Study With GNbAC1 in Healthy Male Volunteers

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
May 25, 2015
Registry last updated
Oct 20, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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