Phase 1b Multiple Ascending Dose Study of Foralumab in Primary and Secondary Progressive MS

NCT ID: NCT05029609

Last Updated: 2022-03-03

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE1
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-10-31
• Study Completion Date: 2022-12-31

Brief Summary

The primary objective is to establish the safety of administration of intranasal Foralumab in non-active primary and secondary progressive Multiple Sclerosis (MS) patients in a multiple ascending dose format in escalating doses for 14 consecutive days.

Detailed Description

This is a Phase 1b double blind, randomized, placebo controlled, dose escalating study evaluating multiple doses of Foralumab via intranasal administration for 14 days in patients with MS.

Up to 55 untreated primary and secondary progressive MS patients will be enrolled, to obtain a total of 48 completed subjects (9 active, 3 placebos per group), allowing for dropouts.

Conditions

Primary Progressive Multiple Sclerosis; Secondary Progressive Multiple Sclerosis; Multiple Sclerosis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Group A

Group A will receive nasal Foralumab Dose 1 daily for 14 days (n=9) or placebo (n=3)

Group Type: OTHER

Intranasal Foralumab Solution

Intervention Type: DRUG

The Aptar Unidose device will be used to deliver foralumab nasal solution intranasally. Foralumab nasal solution is prepackaged in a Type 1 glass vial inside the Unidose device.

Placebo

Intervention Type: DRUG

The placebo nasal solution is the acetate buffer vehicle used for foralumab nasal solution. It will be handled in a manner identical to active drug.

Group B

Group B will receive nasal Foralumab Dose 2 tiw for 14 days (n=9) or placebo (n=3)

Group Type: OTHER

Intranasal Foralumab Solution

Intervention Type: DRUG

The Aptar Unidose device will be used to deliver foralumab nasal solution intranasally. Foralumab nasal solution is prepackaged in a Type 1 glass vial inside the Unidose device.

Placebo

Intervention Type: DRUG

The placebo nasal solution is the acetate buffer vehicle used for foralumab nasal solution. It will be handled in a manner identical to active drug.

Group C

Group C will receive nasal Foralumab Dose 3 daily for 14 days (n=9) or placebo (n=3)

Group Type: OTHER

Intranasal Foralumab Solution

Intervention Type: DRUG

The Aptar Unidose device will be used to deliver foralumab nasal solution intranasally. Foralumab nasal solution is prepackaged in a Type 1 glass vial inside the Unidose device.

Placebo

Intervention Type: DRUG

The placebo nasal solution is the acetate buffer vehicle used for foralumab nasal solution. It will be handled in a manner identical to active drug.

Group D

Group D will receive nasal Foralumab Dose 4 daily for 14 days (n=9) or placebo (n=3)

Group Type: OTHER

Intranasal Foralumab Solution

Intervention Type: DRUG

The Aptar Unidose device will be used to deliver foralumab nasal solution intranasally. Foralumab nasal solution is prepackaged in a Type 1 glass vial inside the Unidose device.

Placebo

Intervention Type: DRUG

The placebo nasal solution is the acetate buffer vehicle used for foralumab nasal solution. It will be handled in a manner identical to active drug.

Interventions

Intranasal Foralumab Solution

The Aptar Unidose device will be used to deliver foralumab nasal solution intranasally. Foralumab nasal solution is prepackaged in a Type 1 glass vial inside the Unidose device.

Intervention Type: DRUG

Placebo

The placebo nasal solution is the acetate buffer vehicle used for foralumab nasal solution. It will be handled in a manner identical to active drug.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Confirmed diagnosis of MS (according to the 2010 McDonald criteria).

2. Age 25-70 years.

3. Clinical diagnosis of non-active primary and secondary MS

4. MRI imaging consistent with a diagnosis of MS at any time point.

5. Score on the Expanded Disability Status Scale (EDSS) of 2.5-6.5

6. Adequate hematologic parameters without ongoing transfusion support:

• Hemoglobin (Hb) ≥ 9 g/dL
• Platelets ≥ 100 x 109 cells/L

7. Creatinine ≤ 1.5 x the upper limit of normal (ULN), or calculated creatinine clearance

≥ 60 mL/minute x 1.73 m2 per the Cockcroft-Gault formula

8. Total bilirubin ≤ 2 times the upper limit of normal (ULN) unless due to Gilbert's disease

9. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 times ULN, or < 5 times ULN for patients with liver metastases

10. QT interval corrected for rate (QTcF) ≤ 470 msec for women and ≤ 450 msec for men on the ECG obtained at Screening

11. Negative serum pregnancy test within 14 days prior to the first dose of study therapy for women of child-bearing potential (WCBP)

13. Ability to provide written informed consent.

Exclusion Criteria

1. Corticosteroid use (oral or intravenous) within the last 30 days.

2. Current use or use in the prior 6 months of MS immunotherapy, interferon, glatiramer acetate, fingolimod, siponimod, dimethyl fumarate or natalizumab or any other chronic immunosuppressive medication

3. Inability to tolerate intranasally administered medications

4. Nasal corticosteroids, nasal antihistamines, nasal flu dosing within the past 30 days.

5. Chronic rhinitis, deviated septum, nasal polyps, history of sinusitis treated within the past 12 months.

6. Active COVID-19 disease; according to FDA guidelines

7. Female patient who is pregnant, lactating, breastfeeding, or planning on becoming pregnant during study.

8. Female patients of childbearing age will undergo a pregnancy test and be excluded from the study if positive.

9. Active malignancy within 5 years.

10. Inflammatory bowel disease, rheumatoid arthritis, systemic lupus erythematosus, asthma, or type 1 diabetes

11. Neutropenia (<500 neutrophils/mL) or other severe immunosuppression

12. Unable or unwilling to comply with protocol requirements.

13. Patients with a history of gadolinium allergy.

14. Screening labs outside of the normal range; EBV IgM positive subjects with clinical signs will not receive study drug.

15. Serious cardiac condition within the last 6 months, such as uncontrolled arrhythmia, myocardial infarction, unstable angina or heart disease defined by the New York Heart Association (NYHA) Class III or Class IV (See Appendix B) or hereditary long QT syndrome

16. Concomitant medication(s) that may cause QTc prolongation or induce Torsades de Pointes, except for antimicrobials that are used as standard of care to prevent or treat infections and other such drugs that are considered by the Investigator to be essential for patient care

17. Known positive for human immunodeficiency virus (HIV), hepatitis B virus surface antigen (HBsAg) or hepatitis C virus (HCV)

18. Any other medical intervention or other condition which, in the opinion of the Principal Investigator, could compromise adherence to study requirements or confound the interpretation of study results

• Minimum Eligible Age: 25 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Tiziana Life Sciences LTD

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

TILS-015

Identifier Type: -

Identifier Source: org_study_id