Single Ascending Doses of HER-096 in Healthy Subjects

NCT ID: NCT05915247

Last Updated: 2023-10-27

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-03-29
• Study Completion Date: 2023-09-29

Brief Summary

This study evaluates the safety and tolerability of HER-096 in healthy volunteer subjects by comparing the effects of active study treatment HER-096 to placebo (0.9% physiological saline). In addition, the pharmacokinetic profile of HER-096 in humans will be investigated. The investigational medicinal products will be administered as a single dose by subcutaneous injection.

Detailed Description

This is a Phase I, double-blind, placebo-controlled, clinical study, in which safety, tolerability and pharmacokinetic profile of HER-096 will be investigated after a subcutaneously (s.c.) administered single ascending doses of HER-096 to healthy volunteer subjects (HVS).

Altogether 60-64 HVS will be enrolled into the study and the study will be conducted in two parts, part 1 being randomised and part 2 being open-label. In part 1, up to 48 young male HVS will be randomised 6:2 either to receive HER-096 or placebo (0.9% physiological saline) solution. In part 1, up to 6 dosing cohorts have been planned with single ascending doses of HER-096. In part 2, 12-16 older and elderly HVS, both males and females, will be administered with single dose of HER-096 to evaluate the blood-brain-barrier penetration of HER-096. The investigational medicinal products (HER-096 or placebo solution) will be administered as a s.c. injection.

The total duration of the study will be up to 36 days for each subject, consisting of screening and treatment period.

Conditions

Parkinson Disease

Study Design

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

Study Groups

Placebo (Part 1)

Corresponding volumes of placebo solution according to the dosing cohort administered as a s.c. injection.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Administered as a single dose via s.c. injection

HER-096 (Part 1)

Single ascending doses of HER-096 up to six dosing cohorts administered as a s.c. injection.

Group Type: ACTIVE_COMPARATOR

HER-096

Intervention Type: DRUG

Administered as a single dose via s.c. injection

HER-096 (Part 2)

A single dose of HER-096 will be administered as a s.c. injection.

Group Type: ACTIVE_COMPARATOR

HER-096

Intervention Type: DRUG

Administered as a single dose via s.c. injection

Interventions

HER-096

Administered as a single dose via s.c. injection

Intervention Type: DRUG

Placebo

Administered as a single dose via s.c. injection

Intervention Type: DRUG

Other Intervention Names

0.9% physiological saline; Sodium chloride 9 mg/ml

Eligibility Criteria

Inclusion Criteria

1. Voluntary and written informed consent and alert and oriented to person, place, time and situation at the time of the informed consent.

2. Sufficient command of the Finnish language.

3. Age 20-45 years for Part 1 and 50-75 years for Part 2.

4. Male sex for Part 1, and male or female for Part 2.

5. Body mass index (BMI) 18-30 kg/m2.

6. Good general health.

Exclusion Criteria

1. Predicted poor compliance with study procedures, restrictions and requirements.

2. Veins unsuitable for repeated venipuncture or cannulation.

3. History or evidence of current clinically significant cardiovascular, pulmonary, renal, hepatic, gastrointestinal, haematological, metabolic-endocrine, neurological, urogenital or psychiatric disorder. Subjects with any type of generalized seizures in adulthood must be excluded. Personal or first-degree family history of congenital long QT syndrome or sudden death of a first-degree relative suspected to be due to long QT syndrome will also exclude the subject.

4. History of any type of cancer, except for the age group of >50 years, where a history of successfully treated cancer may be allowed.

5. Susceptibility to severe allergic reactions, e.g. history of anaphylactic shock.

6. Any condition requiring regular concomitant medication (including non-prescriptional over-the-counter drugs), or likely to need any concomitant medication during the study.

7. Use of any medication that might affect the study results or cause a health risk for the subject within 2 weeks prior to IMP administration.

8. Any clinically significant abnormalities in screening laboratory test results, vital signs or physical examination findings that might influence the results of the study or cause a health risk for the subject if he/she takes part in the study.

9. Coagulopathy, thrombocytopenia, use of anticoagulants or other antithrombotic agents.

10. Positive serology to human immunodeficiency virus antibodies (HIVAgAb), hepatitis C virus antibodies (HCVAb) or hepatitis B surface antigen (HBsAg).

11. Any clinically significant 12-lead ECG abnormality.

12. HR < 45 bpm or > 85 bpm, systolic blood pressure (BP) < 90 mmHg or > 150 mmHg, or diastolic BP < 50 mmHg or > 90 mmHg.

13. History of alcohol or drug abuse within the last 5 years, or current regular use of illicit drugs or excessive use of alcohol.

14. Positive breath test for alcohol or positive urine screening test result for drugs of abuse.

15. Current use of nicotine-containing products of more than 5 cigarettes or equivalent per day, or inability to refrain from using nicotine-containing products.

16. Inability to refrain from consuming caffeine-containing beverages.

17. Participation in any other clinical drug study within 3 months before the IMP administration of this study.

18. Donation of blood within 3 months before the IMP administration.

19. Any medical or surgical procedure planned during the study period.

20. Male subjects who are sexually active with a female partner of childbearing potential and do not agree to use two medically accepted methods of contraception during the study and for three months after the dosing, and refrain from donating sperm during this time.

21. Female subjects for Part 2 need to be postmenopausal for at least one (1) year before participation or be surgically sterilized.

22. For subjects in Part 2, any indication of increased intracerebral pressure by neurological examination at inclusion, or another contraindication for LP.

23. Large tattoo or another condition of the skin or subcutaneous tissue that would prevent reliable assessment of local IREs.

24. Significant risk of suicidal behaviour, defined using the C-SSRS.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Clinical Research Services Turku - CRST Oy

UNKNOWN

Sponsor Role: collaborator

Herantis Pharma Plc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Aleksi Tornio, MD

Role: PRINCIPAL_INVESTIGATOR

Clinical Research Services Turku - CRST Oy

Locations

Clinical Research Services Turku - CRST Oy

Turku, , Finland

Countries

Finland

Other Identifiers

2022-003283-24

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

13-XC-CL

Identifier Type: -

Identifier Source: org_study_id