Effect of RANKL Inhibition on UV-induced Immunosuppression

NCT01978483 | Completed Phase 1

• 1 other identifier: Inno-6030
• Study Type: interventional
• Target: 31
• Locations: 1 country
• Sites: 1

Brief Summary

Ultraviolet (UV) light is part of normal sunlight and has many effects on human skin and health. One of the harmful effects of long-term UV light exposure is that it can cause skin cancer. The mechanism by which UV light causes skin cancer is not entirely understood. One of the ways UV light causes cancer is by modifying DNA molecules in the cells of the skin. Another mechanism involved in cancer formation by UV light is immunosuppression. By this mechanism, UV light inactivates cells of the immune system of the skin. The immune cells are responsible for the detection and destruction of foreign substances and organisms such as bacterias and viruses but they also recognize and destroy cancer cells. UV light is known to prevent cells of the immune system to destroy cancer cells. In laboratory experiments, a medication called denosumab has been shown to diminish the inhibition of ultraviolet-induced suppression of skin immunity. In other words, this medication could block the effect of UV on cells of the immune system and might allow patients taking this drug to be better protected from skin cancer. The objective of this study is to test whether denosumab blocks the immunosuppressive effect of UVB light in healthy subjects. This study is divided into two stages. In the first stage, ten subjects (Cohort 1) will be sensitized to diphenylcyclopropenone (DPCP), a topical sensitizer commonly used for the treatment of alopecia areata and cutaneous warts. By reexposing the subjects to DPCP in incremental doses, dose-response levels of cutaneous hypersensitivity reactions in normal skin will be obtained. This will allow comparison of the normal levels of DPCP-induced cutaneous hypersensitivity (CHS) reaction in non UV-exposed skin (Cohort 1) to the CHS obtained from the two UVB-exposed experimental groups of Cohort 2. In the second stage of the study, 20 subjects (Cohort 2) will be exposed to an immunosuppressive dose of ultraviolet B (UVB) 24 hours prior to DPCP sensitization. This is expected to result in the abolition of CHS upon rechallenge with DPCP. In order to assess whether denosumab can reverse UVB-induced immunosuppression, the subjects will have previously been randomized to receive a single 1mL injection of either 60 mg denosumab (group A; 10 subjects) or 1 mL saline (group B; 10 subjects) two weeks before UVB exposure. CHS reactions elicited by DPCP rechallenge will be compared between the denosumab and saline groups.

Conditions

Ultraviolet Rays; Immunosuppression; Hypersensitivity, Delayed; Immune Tolerance/Drug Effects

Keywords

Humans; Adult; skin; metabolism; radiation effects; Ultraviolet Rays; RANKL; RANK Ligand; denosumab; diphenylcyclopropenone; diphencyprone; immunology; immunosuppression; Antibodies, Monoclonal; Dermatitis, Allergic Contact; Hypersensitivity, Delayed

Outcome Measures

Primary Outcomes (1)

• Change in dermal thickness: denosumab group vs placebo group of Cohort 2

  Mean dermal thickness, as measured by 20 MHz ultrasonography, after challenge with incremental doses of DPCP for subjects randomized to denosumab as compared to subjects randomized to placebo.

  Three weeks after sensitization to DPCP.

Secondary Outcomes (7)

• Clinical score of contact hypersensitivity reactions: denosumab group vs placebo group of Cohort 2

  Three weeks after sensitization to DPCP.

• Diameters of contact hypersensitivity reactions: denosumab group vs placebo group of Cohort 2

  Three weeks after sensitization to DPCP.

• Change in dermal thickness: non UV-exposed (Cohort 1) vs UV-exposed (Cohort 2)

  Three weeks after sensitization to DPCP.

• Clinical score of contact hypersensitivity reactions: non UV-exposed (Cohort 1) vs UV-exposed (Cohort 2)

  Three weeks after sensitization to DPCP.

• Diameters of contact hypersensitivity reactions: non UV-exposed (Cohort 1) vs UV-exposed (Cohort 2)

  Three weeks after sensitization to DPCP.

Study Arms (3)

DPCP alone (Cohort 1)

OTHER

Diphenylcyclopropenone sensitization patches applied for 48hours. Diphenylcyclopropenone elicitation patches applied for 48hours.

Drug: Diphenylcyclopropenone

UVB and denosumab group (Cohort 2)

EXPERIMENTAL

Denosumab 60mg subcutaneous injection once. Broadband UVB exposure once. Diphenylcyclopropenone sensitization patches applied for 48hours. Diphenylcyclopropenone elicitation patches applied for 48hours.

Drug: Denosumab; Radiation: UVB exposure; Drug: Diphenylcyclopropenone

UVB and placebo group (Cohort 2)

PLACEBO COMPARATOR

Normal saline 1mL subcutaneous injection once. Broadband UVB exposure once. Diphenylcyclopropenone sensitization patches applied for 48hours. Diphenylcyclopropenone elicitation patches applied for 48hours.

Radiation: UVB exposure; Drug: Diphenylcyclopropenone; Drug: Normal Saline

Interventions

Denosumab DRUG

Also known as: Prolia

UVB and denosumab group (Cohort 2)

UVB exposure RADIATION

Also known as: Ultraviolet B rays, Ultraviolet B light

UVB and denosumab group (Cohort 2); UVB and placebo group (Cohort 2)

Diphenylcyclopropenone DRUG

Also known as: Diphencyprone, DPCP

DPCP alone (Cohort 1); UVB and denosumab group (Cohort 2); UVB and placebo group (Cohort 2)

Normal Saline DRUG

Also known as: Saline 0.9%, NaCl solution 0.9%

UVB and placebo group (Cohort 2)

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• \. Men or postmenopausal women 18 years of age or older at time of consent.
• \. Male subject or his female partner (this criterion does not apply to post-menopausal female) is willing to use effective contraceptive method for at least 30 days before Day 0 and at least 1 month after the last study drug administration. Effective contraceptive methods are:
• Barrier methods such as condom, sponge or diaphragm combined with spermicide in foam, gel or cream;
• Hormonal contraception (oral, intramuscular, implant or transdermal) which include Depo-Provera, Evra and Nuvaring;
• Intrauterine device (IUD);
• Sterilization such as tubal ligation, hysterectomy or vasectomy;
• Postmenopausal state for at least 1 year for female subject or female partner of male subject;
• Same-sex partner;
• Abstinence.
• \. Capable of giving informed consent and the consent must be obtained prior to any study related procedures.
• \. Fitzpatrick skin phototypes II or III.
• \. Subject weighs 100kg or less.

You may not qualify if:

• \. Conditions or medications causing immunosuppression, photosensitization or phototoxicity.
• \. Past history of skin cancer or subject having precancerous skin lesions (eg. actinic keratosis).
• \. Subject has atopic dermatitis (cohort 1)
• \. Subject has received investigational drugs within the 28 days or 5 half-lives, whichever is longer, prior to Day 0 or plans to during the study period.
• \. Subject has used any topical medication on arms or buttocks within 14 days of Day 0 or plans to during the study.
• \. At the investigator's discretion subject has current or past history of alcohol or drug abuse that would interfere with the ability of the subject to comply with the study protocol.
• \. Hypersensitivity/allergy to denosumab.
• \. Hypersensitivity/allergy to lidocaine.
• \. Hypersensitivity/allergy to latex.
• \. Subject is taking anticoagulant medication except for low dose acetylsalicylic acid.
• \. Past history of hypocalcemia or predisposing factors (eg, history of hypoparathyroidism, thyroid surgery, parathyroid surgery, malabsorption syndromes, excision of small intestine, severe renal impairment or receiving dialysis).
• \. Known vitamin D deficiency.
• \. Creatinine clearance less than 30mL/min (Cohort 2 only).
• \. Corrected calcium concentration inferior to the normal range (Cohort 2 only).
• \. Past history of osteonecrosis of the jaw (ONJ) or risk factors for ONJ (poor oral hygiene, periodontal and/or pre-existing dental disease, diagnosis of cancer with bone lesions, invasive dental procedures such as dental extractions or implants within 6 months of the screening visit.)

Sponsors & Collaborators

• Innovaderm Research Inc.: lead

Study Sites (1)

Innovaderm Research Inc.

Montreal, Quebec, H2K 4L5, Canada

Location

MeSH Terms

Conditions

Hypersensitivity, Delayed; Dermatitis, Allergic Contact

Interventions

Denosumab; RulB protein, Pseudomonas syringae; diphenylcyclopropenone; Saline Solution; Sodium Chloride

Condition Hierarchy (Ancestors)

Hypersensitivity; Immune System Diseases; Dermatitis, Contact; Dermatitis; Skin Diseases; Skin and Connective Tissue Diseases; Skin Diseases, Eczematous

Intervention Hierarchy (Ancestors)

Antibodies, Monoclonal, Humanized; Antibodies, Monoclonal; Antibodies; Immunoglobulins; Immunoproteins; Blood Proteins; Proteins; Amino Acids, Peptides, and Proteins; Serum Globulins; Globulins; Crystalloid Solutions; Isotonic Solutions; Solutions; Pharmaceutical Preparations; Chlorides; Hydrochloric Acid; Chlorine Compounds; Inorganic Chemicals; Sodium Compounds

Study Officials

• Robert Bissonnette, MD

  Innovaderm Research Inc.

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: BASIC SCIENCE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 31, 2013
• First Posted: November 7, 2013
• Study Start: November 1, 2013
• Primary Completion: June 1, 2014
• Study Completion: June 1, 2014
• Last Updated: July 24, 2014

Record last verified: 2014-07

Locations

CA (1)