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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03161288
Other study ID # KY1005-CT01
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date May 29, 2017
Est. completion date March 30, 2018

Study information

Verified date August 2019
Source Kymab Limited
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a single and multiple ascending dose, placebo-controlled, double-blind, Phase 1 study to evaluate the safety and tolerability of KY1005 in healthy volunteers.


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date March 30, 2018
Est. primary completion date March 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

Subjects must fulfil all of the following criteria for entry into the study.

1. Volunteer to participate in the clinical trial and provide signed informed consent.

2. Male, aged 18 to 45 years.

3. Subjects with a female spouse/partner of childbearing potential must agree to use effective birth control starting at screening and continuing throughout the clinical study period and for a period of up to 6 months after study completion.

4. Cohorts 4 to 8: previous immunisation with tetanus toxoid (TT) but not within 6 months prior to the screening visit as reported by the volunteer.

5. Cohorts 4 to 8: anti-TT immunoglobulin G (IgG) response > 0.1 IU/mL and = 50 IU/mL at screening.

Exclusion Criteria:

Subjects fulfilling any of the following exclusion criteria are not eligible for entry into the study.

1. Experiencing a clinically significant, chronic or acute infection requiring treatment at screening or prior to first IMP administration.

2. A body weight of = 60.0 kg or = 120.0 kg.

3. A body mass index = 18.0 or = 30.0 kg/m2.

4. History of disease of the central nervous system, cardiovascular system, kidney, liver, digestive system, respiratory system or metabolic/endocrine system or suffered from other disease that in the opinion of the principal investigator (or medically qualified designee) may make participation unsafe for the subject or interfere with trial evaluations or otherwise considered clinically significant.

5. History of immunological abnormality (e.g., immune suppression, severe allergy or anaphylaxis) that in the opinion of the principal investigator (or medically qualified designee) may make participation unsafe for the subject or interfere with trial evaluations or otherwise considered clinically significant.

6. History of malignancy, or known current malignancy.

7. Leukocyte absolute value < 3.50 × 10^9/L or > 9.50 × 10^9/L, neutrophil absolute value < 1.8 × 10^9/L, platelet counts < 100 × 10^9/L, haemoglobin < 12.0 g/dL.

8. Taken part in other clinical trials within 3 months of screening for this study or > four trials in the year preceding the first IMP administration.

9. Donated or lost more than 500 mL of blood or plasma within 3 months of screening.

10. Prescription drug taken within 2 weeks of screening or likely to be taken during the trial.

11. Live immunisation within 3 months of screening or plans to receive such immunisation during the clinical trial or for a period of 6 months after the end of the trial.

12. Taking or likely to take over-the-counter medication, including herbal medicines, that in the opinion of the principal investigator (or medically qualified designee) may make participation unsafe for the subject or interfere with trial evaluations.

13. Hepatitis B surface antigen, Hepatitis C antibody, or Human Immunodeficiency Virus positive.

14. History of or current drug or substance abuse considered significant by the principal investigator (or medically qualified designee) including a positive urine drug screen.

15. Current smoker and/or regular user of other nicotine-containing products (e.g., patches).

16. Average consumption of more than 14 units of alcohol/week.

17. Clinically significant abnormal screening values in clinical (electrocardiograms (ECGs), vital signs, physical examination) and laboratory tests in the opinion of the principal investigator (or medically qualified designee).

18. Cannot communicate adequately or cannot commit to full participation in all trial procedures.

19. For Cohorts 4 to 8:

1. Confirmed previous exposure to immunocyanins, such as keyhole limpet haemocyanin (KLH);

2. Known allergy to thiomersal or other components of Tetanus vaccine or Immucothel®;

3. History of schistosomiasis.

20. Any observation that, in the opinion of the principal investigator (or medically qualified designee) makes the subject unsuitable for participation in this study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
KY1005
A human anti-OX40 ligand monoclonal antibody
Placebo
Matched placebo

Locations

Country Name City State
Netherlands Centre for Human Drug Research Leiden

Sponsors (1)

Lead Sponsor Collaborator
Kymab Limited

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Other Serum anti-KY1005 antibody titres Change in serum anti-KY1005 antibody titres from pre-infusion. Cohorts 1 to 3: up to day 113. Cohorts 4 to 8: up to day 92.
Other Immunophenotype and OX40/OX40L expression Changes in specific cell subsets and expression of OX40/OX40L on each subset (where evaluable). Cohorts 1- 8: up to day 85.
Other Neo-antigen and recall antigen immunological responses (cohorts 4-8 only) Change in anti-tetanus toxoid immunoglobulin G (IgG) and immunoglobulin M (IgM) titres in serum and anti-Immucothel® IgG and IgM titres in serum. up to day 85
Other Delayed Type Hypersensitivity response in the skin after intradermal injection of Immucothel® or saline measured by Antera 3D® camera image analysis (cohorts 4-8 only) Change in skin colour a and haemoglobin level (concentration of redness per unit area relative to region of interest) Day 85 and 87
Other Delayed Type Hypersensitivity response in the skin after intradermal injection of Immucothel® or saline measured by LSCI photography (cohorts 4-8 only) Change in basal flow and flare Day 85 and 87
Primary Occurrence of all treatment-related adverse events Cohorts 1 to 3: up to day 113. Cohorts 4 to 8: up to day 92.
Primary Changes in vital signs (as a measure of safety and tolerability) Cohorts 1 to 3: from pre-first infusion up to day 113. Cohorts 4 to 8: from pre- first infusion up to day 92.
Primary Changes in laboratory safety data (as a measure of safety and tolerability) Cohorts 1 to 3: from pre-first infusion up to day 113. Cohorts 4 to 8: from pre-first infusion up to day 92.
Primary Changes in anti-viral antibody levels and viral DNA (as a measure of safety and tolerability) Cohorts 1 to 3: from pre-first infusion up to day 113. Cohorts 4 to 8: from pre-first infusion up to day 92.
Primary Changes in acute cytokines (as a measure of safety and tolerability) Cohorts 1 to 3: from pre-first infusion up to day 113. Cohorts 4 to 8: from pre-first infusion up to day 92.
Primary Changes in electrocardiograms (as a measure of safety and tolerability) Cohorts 1 to 3: from pre-first infusion up to day 113. Cohorts 4 to 8: from pre-first infusion up to day 92.
Secondary Maximum observed serum concentration (Cmax) following the first, second and third infusions for each KY1005 dose/dosing group Cohorts 1 to 3: up to day 113. Cohorts 4 to 8: up to day 92.
Secondary Time to maximum observed serum concentration (tmax) following the first, second and third infusions for each KY1005 dose/dosing group Cohorts 1 to 3: up to day 113. Cohorts 4 to 8: up to day 92.
Secondary Trough concentrations (Cmin) following the first and second infusions and 28 days after the third infusion Cohorts 1 to 3: up to day 113. Cohorts 4 to 8: up to day 92.
Secondary Areas under the plasma concentration-time curves (AUC) Cohorts 1 to 3: up to day 113. Cohorts 4 to 8: up to day 92.
Secondary Clearance (CL) Cohorts 1 to 3: up to day 113. Cohorts 4 to 8: up to day 92.
Secondary Apparent volume of distribution during terminal phase (Vz) Cohorts 1 to 3: up to day 113. Cohorts 4 to 8: up to day 92.
Secondary Apparent volume of distribution at steady state (Vss) Cohorts 1 to 3: up to day 113. Cohorts 4 to 8: up to day 92.
Secondary Half-life (t½) Cohorts 1 to 3: up to day 113. Cohorts 4 to 8: up to day 92.
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