Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of CC-90006 in Subjects With Mild to Moderate Plaque-type Psoriasis

Psoriasis Clinical Trial

Official title:

A Phase 1, Multi-center, Randomized, Double-blind, Placebo-controlled, Multiple-dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CC-90006 Administered Subcutaneously in Patients With Plaque-type Psoriasis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03337022
• Other study ID #: CC-90006-CP-002
• Status: Completed
• Phase: Phase 1
• Start date: January 4, 2018
• Est. completion date: April 26, 2019

Study information

• Verified date: May 2020
• Source: Celgene
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multi-center, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, Pharmacokinetics (PK), Pharmacodynamics (PD), and immunogenicity of CC-90006 following administration of multiple subcutaneous doses in subjects with mild to moderate plaque-type psoriasis.

Description:

The study will be conducted in subjects with mild to moderate plaque-type psoriasis.

The study will consist of escalating multiple (three) doses in sequential groups. Approximately 40 subjects with plaque-type psoriasis will be enrolled into approximately 4 planned dose cohorts.

Each cohort will study a different CC-90006 dose level and have ten subjects; eight subjects will receive CC-90006 and two subjects will receive placebo. Subjects will be dosed according to a computer-generated randomization scheme. Dosing will occur on Days 1, 15 (Week 2), and 29 (Week 4). During the study, blood samples and punch biopsies will be collected to determine the amount of CC-90006 in the body and to evaluate its effect on the subject's condition. Subjects will return to the clinic for regular follow up visits for safety, PK, and PD. A follow up phone call to each subject to determine general health will occur on Day 141 (week 20).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 34
• Est. completion date: April 26, 2019
• Est. primary completion date: April 26, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

The following is a summary of the inclusion criteria:

1. Males or non-pregnant females between the ages of 18 and 60 years (inclusive) at the time of signing the ICF, and be willing to adhere to the requirements of contraception use throughout the study.

1. Female subjects who claim to be surgically sterile (hysterectomy, bilateral oophorectomy, or bilateral salpingo-oophorectomy; proper documentation required) must have undergone the procedure at least 6 months before screening,

2. Females who claim to be postmenopausal (defined as 24 consecutive months without menses before screening, should have a confirmed follicle-stimulating hormone [FSH] level of > 40 IU/L at screening).

3. All other females must:

i. Have two negative pregnancy tests (at screening and baseline) as verified by the Investigator prior to starting study treatment. She must agree to ongoing pregnancy testing during the course of the study, and after end of study treatment. This applies even if the subject practices true abstinence from heterosexual contact.

ii. Either commit to true abstinence from heterosexual contact or agree to use two forms of reliable contraception simultaneously. One must be a highly effective method and one additional effective (barrier) method, and both must be practiced without interruption, 28 days prior to starting investigational product, during the study therapy (including dose interruptions), and for 4 months after discontinuation of study therapy.

d. Males must practice true abstinence1 (which must be reviewed on a monthly basis and source documented) or agree to use a barrier method of birth control (condoms not made out of natural [animal] membrane [latex condoms are recommended]) during sexual contact with a pregnant female or FCBP2 while participating in the study, during dose interruptions, and for at least 4 months after the last dose of IP, even if he has undergone a successful vasectomy.

2. Must be diagnosed with mild to moderate plaque-type psoriasis at least 6 months prior to baseline (Day 1).

3. Must have a PASI = 15 at screening and baseline (Day 1).

4. Must have a body surface area affected score (BSA) = 1 and sPGA = 3 at screening and baseline (Day 1).

5. Must have at least two plaques, at least 3 x 3 centimeters(cm) in diameter. One plaque will be used for punch biopsy and the other for TPSS evaluation.

6. Other than the diagnosed condition of mild to moderate plaque-type psoriasis, the subject must be in good health as determined by a physical examination (PE) at screening.

7. Has a body mass index (BMI) = 18 and = 35 kg/m2 at screening.

8. For all other clinical laboratory safety test parameters, the subject has results within normal limits or judged to be not clinically significant by the Investigator.

Exclusion Criteria:

The following is a summary of the exclusion criteria:

1. Presence of any significant medical condition, laboratory abnormality, or psychiatric illness which places him or her at unacceptable risk by participating in the study, or that would that would prevent the subject from participating in the study for other reasons, or would confound the ability to interpret data from the study.

2. History of cancer.

3. Presence of cancer or pre-cancerous conditions,

4. Presence of confirmed cervical dysplasia.

5. Presence of a systemic infection or any potentially opportunistic infections (eg, atypical mycobacterial, CMV, Clostridium difficile, multifocal herpetic, etc).

(Immunologic disorders such as rheumatoid arthritis, lupus, asthma, and any immunodeficiency are exclusionary.)

6. Presence of latent tuberculosis infection and/or active tuberculosis disease, as tested using QuantiFERON-TB Gold test (or equivalent). Subjects with a history of TB who have completed treatment (documented) may be eligible for the study.

7. History of serum hepatitis, or a confirmed carrier of hepatitis B surface antigen (HBsAg), or hepatitis B core antibody (HBcA), or hepatitis C virus antibody (HCV Ab), or who has a positive HIV antibody test.

8. Presence of non-plaque psoriasis (erythrodermic, guttate, inverse, or pustular psoriasis).

9. Presence of dermatological diseases other than plaque psoriasis, including but not limited to seborrheic dermatitis, lichen simplex chronicus, atopic dermatitis, nummular eczema, superficial fungal infections, subacute cutaneous lupus erythematosus, pityriasis rubra pilaris, crusted scabies, cutaneous T cell lymphoma

10. Use of topical therapy for psoriasis within 14 days of first dosing (including but not limited to corticosteroids, retinoids, vitamin D analog, calcineurin inhibitors, salicylic acid).

11. Use of systemic therapy for psoriasis within 30 days of first dose administration.

12. Use of phototherapy for psoriasis within 30 days of first dose administration.

13. Use of systemic biologics treatment for psoriasis within 24 weeks of first dose administration.

14. Exposure to an immunosuppressive or immunomodulatory drug within 30 days of first dose administration, or five half-lives of the drug (whichever is longer).

15. Exposure to an investigational drug (new chemical entity) within 30 days preceding the first dose administration, or five half-lives of that investigational drug, if known (whichever is longer).

16. Smoking > 10 cigarettes per day, or the equivalent in other tobacco products (self-reported).

17. Vaccination within 30 days prior to the first dose administration or subject has plans to receive a vaccination during the course of the study.

Related Conditions & MeSH terms

• Psoriasis

Intervention

Drug:
• CC-90006
CC-90006

Other:
• Placebo
Placebo

Locations

Country	Name	City	State
Canada	Innovaderm Research	Montreal	Quebec
United States	Anaheim Clinical Trials, LLC	Anaheim	California
United States	Altoona Center for Clinical Research	Duncansville	Pennsylvania
United States	TKL Research	Fair Lawn	New Jersey

Sponsors (1)

Lead Sponsor	Collaborator
Celgene

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Adverse Events (AEs)	Number of participants with adverse events	Up to approximately Week 20
Secondary	Pharmacokinetics: Cmax	Observed maximum concentration of CC-90006 in serum	Up to approximately 16 weeks
Secondary	Pharmacokinetics - Tmax	Time to reach the observed maximum concentration of CC-90006 in serum	Up to approximately 16 weeks
Secondary	Pharmacokinetics - AUC 0-t	Area under that serum-concentration time curve calculated from time zero to the last measured time point	Up to approximately 16 weeks
Secondary	Pharmacokinetics - AUC 0-8	Area under that serum-concentration time curve calculated from time zero to 8	Up to approximately 16 weeks
Secondary	Pharmacokinetics - t1/2	Terminal elimination half-life	Up to approximately 16 weeks
Secondary	Pharmacokinetics - CL/F	Apparent clearance of drug from serum after extravascular administration	Up to approximately 16 weeks
Secondary	Pharmacokinetics - Vz/F	Apparent volume of distribution during the terminal phase	Up to approximately 16 weeks
Secondary	Pharmacokinetics - Rac [AUCt]	Accumulation ratio based on Cmax (Rac [Cmax]) and AUCt	Up to approximately 16 weeks
Secondary	Fraction of subjects with Anti-drug antibody (ADA)	Measure of the body's immune response to CC-90006	Up to approximately 16 weeks