A Randomized Placebo-Controlled Study of the Neurokinin-1 (NK1) Receptor Antagonist Serlopitant Prurigo Nodularis (PN)

Prurigo Nodularis Clinical Trial

Official title:

A Randomized, Double-Blind, Placebo-Controlled, Study of Neurokinin-1 Receptor Antagonist Serlopitant in Subjects With Prurigo Nodularis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02196324
• Other study ID #: TCP-102
• Status: Completed
• Phase: Phase 2
• Start date: July 9, 2014
• Est. completion date: June 10, 2016

Study information

• Verified date: May 2021
• Source: Vyne Therapeutics Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to demonstrate whether or not VPD-737, an NK1 receptor antagonist is safe and effective for treatment of prurigo nodularis versus placebo.

Description:

The sensation of itch is transmitted to the brain through the nervous system. Several chemicals are involved in transmitting this signal.This trial of VPD 737 is intended to treat this condition by blocking one of the chemicals involved in the transmission of the itch signal. This is an oral drug administered once daily It has been used in other trials and has shown to be safe at the doses used in this trial. The trial will involve once daily pills for 8 weeks. Subject will be asked to fill out questionnaires both electronically and on paper during the study period. Patients will also be monitored for safety and will have blood taken for testing and several points during the trial. Overall participation will last about 14 weeks

Recruitment information / eligibility

• Status: Completed
• Enrollment: 128
• Est. completion date: June 10, 2016
• Est. primary completion date: May 27, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Subjects meeting all of the following criteria will be eligible for study entry:

1. Males or females who are at least 18 years and no more than 80 years of age at Screening.

2. Must have PN (defined as the presence of pruritic nodules due to chronic pruritus,) of more than 6 weeks duration despite treatment with current therapies such as antihistamines or corticosteroids ("treatment resistant" PN).

3. Must have PN lesions on both arms, both legs, and/or the trunk (ie, the lesions must not be localized).

4. Must have a VAS pruritus score of 70 or greater within 72 hours of Baseline.

5. Males, non-fecund females (ie, surgically sterilized, if procedure was done 12 months before screening or subject is postmenopausal, without menses for 12 months before screening), or females of childbearing potential using an acceptable method of birth control for a period of 35 days before the first dosing, and all females must have a negative pregnancy test at the screening and baseline visits:

Note 1: Acceptable methods of birth control include any one of the following:

abstinence, vasectomized sexual partner, hormonal methods (ie, birth-control pill, hormonal IUD, Depo-Provera, implants, patch, intravaginal device [NuvaRing]), intrauterine device (IUD [copper banded coils]), diaphragm, cervical cap, or condom with spermicidal jelly or foam. Subjects using oral contraceptives must also use a reliable backup method of birth control during the study and until the first menses after the last dose of study medication or for 14 days menses after the last dose of study medication.

6. Willing and able to understand and provide written informed consent.

7. Willing and able to comply with study requirements and restrictions including the discontinuation of all current therapies for pruritus.

8. Subjects must be in good health as determined by medical history, physical examination, and results of Electro Cardio Gram (ECG) and clinical laboratory tests (including urinalysis).

9. Agreeing to confidential use and storage of all data and use of all anonymized data for publication including scientific publication.

Exclusion Criteria:

• Subjects not eligible for the study are those who:

• Have chronic pruritus due conditions other than PN, such as the following conditions:

• Lichen simplex chronicus

• Lichen amyloidosus

• Localized pruritus (e.g., only one arm affected)

• Neuropathic and psychogenic pruritus (notalgia paresthetica, brachioradial pruritus, somatoform prurigo, dilusional parasitosis, depression associated prurigo)

• Active dermatoses needing immediate therapy such as atopic dermatitis (without PN) or bullous pemphigoid;

• Have a history of use (within the specified time periods) of the medications listed below. Prior to randomization, a subject who used any of these medications must undergo a washout period equal to the length of the interval specified below (eg, 2 weeks for antihistamines, 4 weeks for naltrexone, and 4 weeks for cyclosporine A).

• Topical or systemic antihistamines, (used =2 weeks prior to the baseline visit) [loratindine, or cetirizine may act as rescue medication during treatment];

• Topical calcineurin inhibitors, topical capsaicin, menthol, camphor, polidocanol, topical antibiotics, antiseptic baths and cleansing lotions (used =2 weeks prior to the baseline visit);

• Topical steroids (used =2 weeks prior to the baseline visit);

• Naltrexone, paroxetine, fluvoxamine, amitriptyline, gabapentin, pregabalin, or UVtherapy (prescribed for the pruritus treatment) (used =4 weeks prior to the baseline visit);

• Systemic steroids (used =4 weeks prior to the baseline visit);

• Cyclosporine A and other immunosuppressants (used =4 weeks prior to the baseline visit).

• Have any medical condition or disability that would interfere with the assessment of safety or efficacy in this trial or would compromise the ability of the subject to undergo study procedures or to give informed consent.

• Have any chronic or acute medical condition that, in the opinion of the investigator, might interfere with the study results or place the subject at undue risk.

• Have a history of sensitivity to any components of the study material.

• Are females of childbearing potential who are unwilling to use adequate contraception or who are breast feeding.

• Have chronic renal disease, ie, serum creatinine greater than 2.4 mg/dL.

• Have aspartate aminotransferase (AST) or alanine aminotransferase (ALT) greater than 2 times the upper limit of normal. Subjects with hepatitis B or C who have normal liver function may be enrolled.

• Have a current malignancy (such as Hodgkin's lymphoma, B or T cell lymphoma, or myeloma) or blood cell dyscrasia (eg, polycythemia or myelofibrosis) that might lead to systemic chronic pruritus.

• Subjects with untreated hyperthyroidism.

• Have pruritus of psychiatric etiology (eg, delusions of parasitosis, obsessive compulsive disorder, or major depression) or neuropathic etiology (eg, due to shingles, spinal cord injury or with neurologic deficit).

• Have pruritus due to urticaria, drug allergy, or infection (such as pityriasis rosea or tinea or active human immunodeficiency virus [HIV]). Note: Subjects with HIV who have undetectable viral load, CD 4 counts >200 cells/cc, and stable retroviral therapy may enroll.

• Are on medications known to cause pruritus (ie, Erbitux®, opioids, cocaine, amphetamines, and angiotensin converting enzyme [ACE] inhibitors) and are suspected of having drug-induced pruritus.

• Have taken investigational medications within 30 days prior to Screening.

• Are currently participating in any other clinical study.

• Have a history (within the previous 4 weeks) of use of tricyclic antidepressants, selective serotonin reuptake inhibitors (SSRI), serotonin-norepinephrine reuptake inhibitors (SNRIS), monoamine oxidase (MAO) inhibitors, opioids, immunemodulators (e.g. azathioprine, methotrexate, mycophenolate mofetil, cyclosporine A, antibodies), or neuroactive medications (e.g. pregabalin, gabapentin).

• Have a history (within the previous 4 weeks) of use of sedatives or tranquilizers.

Subjects must undergo an appropriate washout period from any sedatives or tranquilizers before enrolling in the study.

• Are currently treated with strong CYP3A4 inhibitors (e.g. conazole, ketoconazole, fluconazole, itraconazole, voroconazole etc. or erythromycin). The co-administration of moderate CYP3A4 inhibitors to VPD-737 may be allowed with investigator agreement and appropriate safety monitoring.

• Received ultraviolet B (UVB) or psoralen + ultraviolet A (PUVA) treatment within 30 days prior to Screening.

• Within the past 12 months, have expressed suicidal ideation with some intent to act.

• Started or changed creams, or emollients including over-the-counter (OTC) preparations or bath oil treatment for relief of pruritus within 2 weeks prior to Screening.

• Have any social or medical condition (eg, alcoholism, drug dependency, psychotic state) that, in the investigator's opinion, might interfere with the subject's ability to comply with the requirements of the protocol.

• Are employees of the study site or of the Sponsor's company.

Related Conditions & MeSH terms

• Neurodermatitis
• Prurigo
• Prurigo Nodularis

Intervention

Drug:
• serlopitant
NK1 receptor antagonist
• Placebo
Placebo

Locations

Country	Name	City	State
Germany	Study Site 07	Berlin-Mitte
Germany	Study Site 08	Bonn
Germany	Study Site 06	Dresden
Germany	Study Site 12	Dusseldorf
Germany	Study Site 02	Frankfurt
Germany	Study Site 09	Hamburg
Germany	Study Site 05	Heidelberg
Germany	Study Site 03	Kiel
Germany	Study Site 11	Leipzig
Germany	Study Site 04	Lubeck
Germany	Study Site 14	Mainz
Germany	Study Site 01	Muenster
Germany	Study Site 16	München
Germany	Study Site 15	Selters
Germany	Study Site 10	Tübingen

Sponsors (1)

Lead Sponsor	Collaborator
Vyne Therapeutics Inc.

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Average Visual Analog Scale at Baseline	At study visits, participants recorded a mark for pruritus severity on a 10-cm horizontal line. This thermometer-type scale was marked with ratings of "no itch" (0 cm) and worst imaginable itch" (10 cm). Average Visual Analog Scale (VAS) (average itch over the past 24 hours) was recorded. Higher scores indicated worse outcome.	At Baseline
Primary	Average Visual Analog Scale at Week 2	At study visits, participants recorded a mark for pruritus severity on a 10-cm horizontal line. This thermometer-type scale was marked with ratings of "no itch" (0 cm) and worst imaginable itch" (10 cm). Average VAS (average itch over the past 24 hours) was recorded. Higher scores indicated worse outcome.	At Week 2
Primary	Average Visual Analog Scale at Week 4	At study visits, participants recorded a mark for pruritus severity on a 10-cm horizontal line. This thermometer-type scale was marked with ratings of "no itch" (0 cm) and worst imaginable itch" (10 cm). Average VAS (average itch over the past 24 hours) was recorded. Higher scores indicated worse outcome.	At Week 4
Primary	Average Visual Analog Scale at Week 8	At study visits, participants recorded a mark for pruritus severity on a 10-cm horizontal line. This thermometer-type scale was marked with ratings of "no itch" (0 cm) and worst imaginable itch" (10 cm). Average VAS (average itch over the past 24 hours) was recorded. Higher scores indicated worse outcome.	At Week 8
Secondary	Number of Participants With Improvement in Pruritus as Reported on Verbal Rating Scale (VRS) - Pruritus	At study visits, participants used the VRS to rate their skin sensations (pruritus, burning, and stinging) using a 5-point scale (0 = not present; 1 = mild present; 2 = moderately present; 3 = severely present; and 4 = very severely present). Higher scores indicated worse outcome.	At Baseline and Week 8
Secondary	Number of Participants With Improvement in Burning as Reported on Verbal Rating Scale (VRS) - Burning	At study visits, participants used the VRS to rate their skin sensations (pruritus, burning, and stinging) using a 5-point scale (0 = not present; 1 = mild present; 2 = moderately present; 3 = severely present; and 4 = very severely present). Higher scores indicated worse outcome.	At Baseline and Week 8
Secondary	Number of Participants With Improvement in Stinging as Reported on Verbal Rating Scale (VRS) - Stinging	At study visits, participants used the VRS to rate their skin sensations (pruritus, burning, and stinging) using a 5-point scale (0 = not present; 1 = mild present; 2 = moderately present; 3 = severely present; and 4 = very severely present). Higher scores indicated worse outcome.	At Baseline and Week 8
Secondary	Worst Visual Analog Scale (VAS)	At study visits, participants recorded a mark for pruritus severity on a 10-cm horizontal line. This thermometer-type scale was marked with ratings of "no itch" (0 cm) and worst imaginable itch" (10 cm). Worst VAS (worst itch over the past 24 hours) was recorded. Higher scores indicated worse outcome.	At Baseline, Weeks 2, 4, and 8
Secondary	Number of Participants With Improvement in Pruritus as Reported on Patient Global Assessment (PGA)	The PGA included a question: Did the pruritus improve during the treatment period (yes/no).	At Weeks 2, 4, and 8
Secondary	Numeric Rating Scale (NRS)	Numeric Rating Scale: Using the patient diary, participants rated the following using an 11-point NRS (0 = no itching; to 10 = worst itch imaginable): average itching over the past 24 hours (Average NRS). Higher scores indicated worse outcome.	At Baseline, Weeks 2, 4, and 8
Secondary	Dermatology Life Quality Index (DLQI)	At each visit, participants completed a DLQI questionnaire. The DLQI is a validated questionnaire consisting of 10 questions relating to the degree to which the participant's skin condition affected his/her daily activities. The DLQI questionnaire is designed for use in adults, i.e. participants over the age of 16.; The scoring of each question is as follows: Very much: scored 3, A lot: scored 2, A little: scored 1, Not at all: scored 0, Not relevant: scored 0, Question 7, 'prevented work or studying': scored 3.; The DLQI is calculated by summing the score of each question resulting in a maximum of 30 and a minimum of 0. The higher the score, the more quality of life is impaired.; Interpreting the DLQI Scores: 0 - 1: no effect at all on participant's life, 2 - 5: small effect on participant's life, 6 - 10: moderate effect on participant's life, 11 - 20: very large effect on participant's life, 21 - 30: extremely large effect on participant's life.	At Baseline, Weeks 2, 4, and 8
Secondary	Pruritus-specific Quality of Life (ItchyQoL)	At each visit, participants completed an ItchyQoL questionnaire. The ItchyQoL is a validated questionnaire consisting of 22 questions based on the concerns and issues pertinent to participants with pruritus.; Items should be scored for the following answers: Never: 1, Rarely: 2, Sometimes: 3, Often: 4, All the time:5. Higher scores indicated worse outcome. Total Score is obtained by calculating the unweighted mean of all ItchyQoL questions.	At Baseline, Weeks 2, 4, and 8
Secondary	Patient Benefit Index, Version for Patients With Pruritus (PBI-P)	At Visits 2 and 5 (or Early termination) only, participants completed the standardized and validated PBI-P questionnaire. Prior to treatment, the first page of the questionnaire, the Patient Needs Questionnaire (PNQ), was administered to determine how different benefits of therapy were relevant for the individual participant. After treatment, using the Patient Benefit Questionnaire (PBQ), participants were asked to evaluate the extent to which the benefits they indicated were important to them were, in fact, realized. From all the items taken together, a weighted total benefit value was calculated, which represented the patient relevant therapy benefits. The mean score greater than 1 is considered to represent a clinically relevant improvement. The items are rated on a 5-point scale with values from 0 (not at all) to 4 (very), allowing for "does/did not apply to me" = 5; and missing value = -9. Higher scores indicated better outcome.	At Week 8 / End of Treatment
Secondary	Number of Participants With Improvement in PN Lesions as Reported on Investigator Global Assessment (IGA)	Using the IGA, physicians rated change in PN lesions (if any) from +5 ("markedly improved") to -5 ("markedly worse"). Higher scores indicated better outcome.	At Week 8
Secondary	Number of Participants With Improvement on Prurigo Activity Score (PAS)	Using the PAS, physicians described, localized, counted, and measured PN lesions.; One of the 7 items was: Activity Stage (Stage 0-4: 0 = 0%, 1 = 1-25%, 2 = 26-50%, 3 = 51-75%, 4 = > 75%); a. Prurigo lesions with excoriations/crusts; Participants with PAS activity stage (prurigo lesions with excoriations/crusts) is presented in the below table.	At Day 1 and Week 8
Secondary	Participants With Rescue Medication Usage	Rescue medications included cetirizine hydrochloride, desloratadine, levocetirizine, and loratadine.	Pre-treatment, upto 8 Weeks
Secondary	Number of Participants With Adverse Events (AEs)	An AE was defined as any untoward medical occurrence associated with the use of a drug in humans, whether or not considered drug related. An AE (also referred to as an adverse experience) could be any unfavorable and unintended sign (eg, an abnormal laboratory finding), symptom, or disease temporally associated with the use of a study drug, without any judgment about causality.	From the time of informed consent (Screening) until the last study visit (follow-up phone call, Week 10)