A Single Ascending Dose Study of GZ402668 in Patients With Progressive Multiple Sclerosis

Progressive Multiple Sclerosis Clinical Trial

Official title:

A Randomized, Double-blind, Placebo-controlled Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of a Single Subcutaneous Dose of GZ402668 in Men and Women With Progressive Multiple Sclerosis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02977533
• Other study ID #: TDU14981
• Secondary ID: 2016-002415-18U1
• Status: Completed
• Phase: Phase 1
• Start date: December 1, 2016
• Est. completion date: May 16, 2018

Study information

• Verified date: April 2022
• Source: Sanofi
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Primary Objective:

To assess the safety and tolerability of GZ402668 after a single subcutaneous (SC) dose in men and women with progressive multiple sclerosis.

Secondary Objectives:

To assess in men and women with progressive multiple sclerosis:

• The pharmacokinetic (PK) parameters of GZ402668 after a single SC dose.

• The pharmacodynamic (PD) response to GZ402668 after a single SC dose.

Description:

The total study duration from screening for a patient can be approximately up to 8 weeks. Upon completion of this trial, patients treated with GZ402668 will be required to enroll in a 4 year safety follow-up study for continued safety observation.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: May 16, 2018
• Est. primary completion date: May 16, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion criteria :

• Male or female adult with a diagnosis of progressive multiple sclerosis (MS) including primary progressive MS, secondary progressive MS, or progressive relapsing MS.

• Aged between 18 and 65 years, inclusive.

• Body weight greater than 40.0 kg.

• Female patients of child bearing potential must use 2 highly effective contraception methods.

• Male patients, whose partners are of childbearing potential (including lactating women), must accept to use, during sexual intercourse, 2 highly effective contraception methods. Males patient, whose partners are pregnant, must use, during sexual intercourse, a condom from the inclusion up to 4 months after investigational medicinal product administration.

• Males patient who has agreed not to donate sperm for 4 months after product administration.

Exclusion criteria:

• Significant medical diseases or conditions, including poorly controlled hypertension, cardiovascular disease, inflammatory disorders, immunodeficiency, autoimmune disease, renal failure, liver dysfunction, cancer (except treated basal skin cell carcinoma), or active infection.

• Frequent headaches and/or migraine, recurrent nausea and/or vomiting.

• History or presence of drug or alcohol abuse.

• Smoking more than 5 cigarettes or equivalent per day.

• If female, pregnancy, lactating, or breast-feeding.

• Patients with relapsing-remitting MS.

• Treatment with natalizumab, methotrexate, azathioprine, or cyclosporine in the past 6 months.

• Treatment with mitoxantrone, cyclophosphamide, cladribine, rituximab or any other immunosuppressant or cytotoxic therapy (other than steroids) in the last 12 months, or determined by the treating physician to have residual immune suppression from these treatments.

• Treatment with glatiramer acetate or interferon beta in the past 4 weeks.

• Treatment with fingolimod within the past 2 months.

• Treatment with dimethyl fumarate in past 4 weeks.

• Treatment with teriflunomide within the past 12 months unless patient has completed an accelerated clearance with cholestyramine.

• Previous treatment with alemtuzumab.

• Live, attenuated vaccine within 3 months prior to the randomization visit, such as varicella-zoster, oral polio, and rubella vaccines.

• Clinically significant abnormality in thyroid function.

• Inability to undergo magnetic resonance imaging with gadolinium administration.

• Hypersensitivity or contraindication to acyclovir.

• Known bleeding disorder.

• Significant autoimmune disease.

• Active infection or at high risk for infection.

• Latent or active tuberculosis.

• Major psychiatric disorder that is not adequately controlled by treatment.

• Epileptic seizures that are not adequately controlled by treatment.

• Prior history of invasive fungal infections.

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Related Conditions & MeSH terms

• Multiple Sclerosis
• Multiple Sclerosis, Chronic Progressive
• Progressive Multiple Sclerosis
• Sclerosis

Intervention

Drug:
• GZ402668
Pharmaceutical form: solution Route of administration: subcutaneous
• Placebo
Pharmaceutical form: solution Route of administration: subcutaneous
• Acyclovir
Pharmaceutical form: tablet Route of administration: oral

Locations

Country	Name	City	State
Germany	Investigational Site Number 276001	Berlin

Sponsors (1)

Lead Sponsor	Collaborator
Sanofi

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants with treatment emergent adverse events		4 weeks
Secondary	Assessment of PK parameter: maximum concentration (Cmax)		4 weeks
Secondary	Assessment of PK parameter: area under curve (AUC)		4 weeks
Secondary	Number of participants with lymphocyte depletion		4 weeks
Secondary	Number of participants with anti-drug antibodies		4 weeks
Secondary	Number of participants with injection site reactions		4 weeks