Trial record 2 of 2 for:
ARQ-154
Safety and Efficacy of ARQ-154 Foam in Subjects With Seborrheic Dermatitis
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT04091646 |
|
Recruitment Status :
Recruiting
First Posted : September 17, 2019
Last Update Posted : January 2, 2020
|
Sponsor:
Arcutis Biotherapeutics, Inc.
Information provided by (Responsible Party):
Arcutis Biotherapeutics, Inc.
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Brief Summary:
This study will assess the safety and effIcacy of ARQ-154 foam vs placebo applied once a day for 56 days by subjects with seborrheic dermatitis
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Seborrheic Dermatitis | Drug: ARQ-154 foam 0.3% | Phase 2 |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 150 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | A Phase 2b, 8-Week, Parallel Group, Double Blind, Vehicle-Controlled Study of the Safety and Efficacy of ARQ-154 Foam 0.3% Administered QD in Subjects With Seborrheic Dermatitis |
| Actual Study Start Date : | October 31, 2019 |
| Estimated Primary Completion Date : | February 2020 |
| Estimated Study Completion Date : | April 2020 |
Resource links provided by the National Library of Medicine
MedlinePlus related topics:
Dandruff, Cradle Cap, and Other Scalp Conditions
| Arm | Intervention/treatment |
|---|---|
| Active Comparator: ARQ-154 foam 0.3% |
Drug: ARQ-154 foam 0.3%
experimental |
| Placebo Comparator: ARQ-154 foam Vehicle |
Drug: ARQ-154 foam 0.3%
experimental |
Primary Outcome Measures :
- Investigator Global Assessment Scale (IGA) Score Change [ Time Frame: 8 Weeks ]Achievement of an IGA score of 'clear' or 'almost clear' plus a 2-grade improvement from Baseline. This global assessment scale has five severity grades reported from 0-4 and defined as Clear (0), Almost Clear (1), Mild (2), Moderate (3), Severe (4).
Secondary Outcome Measures :
- IGA Score Change [ Time Frame: Baseline, Week 2 and Week 4 ]Achievement of an IGA score of 'clear' or 'almost clear' plus a 2-grade improvement from Baseline at weeks 2 and 4. This global assessment scale has five severity grades reported from 0-4 and defined as Clear (0), Almost Clear (1), Mild (2), Moderate (3), Severe (4).
- Overall Assessment of Erythema Score [ Time Frame: Baseline, Week 2, Week 4, Week 8 ]Change from Baseline in Overall Assessment of Erythema score at each study visit. Achievement of an Overall Assessment of Erythema score of 0 or 1 plus a 2-grade improvement from Baseline. This assessment scale has four severity grades reported from 0-3 and defined as None (0), Mild (1), Moderate (2), Severe (3).
- Overall Assessment of Scaling Score [ Time Frame: Baseline, Week 2, Week 4, Week 8 ]Change from Baseline in Overall Assessment of Scaling score at each study visit. Achievement of an Overall Assessment of Scaling score of 0 or 1 plus a 2-grade improvement from Baseline. This assessment scale has four severity grades reported from 0-3 and defined as None (0), Mild (1), Moderate (2), Severe (3).
- Worst Itch Numeric Rating Scale (WI-NRS) Score Change [ Time Frame: Baseline, Week 2, Week 4, Week 8 ]Change in WI-NRS pruritus score from Baseline. In subjects with a Baseline WI-NRS pruritis score of > 6, achievement of a > 4-point improvement from Baseline. WI-NRS is a subject-reported severity of itch at its highest intensity during the previous 24-hour period. The scale is from '0 to 10' ("no itch" to "worst imaginable itch")
Information from the National Library of Medicine
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Participants legally competent to sign and give informed consent.
- Males and females ages 18 years and older (inclusive) at the time of consent.
- Clinical diagnosis of seborrheic dermatitis of at least 3 months duration as determined by the Investigator. Stable disease for the past 4 weeks.
- Seborrheic dermatitis of the scalp and/or face and/or trunk and/or intertriginous areas
- An Investigator Global Assessment (IGA) of disease severity of at least Moderate ('3') at Baseline.
- Overall Assessment of Erythema and Overall Assessment of Scaling scores of Moderate ('2') at Baseline.
- Females of childbearing potential (FOCBP) must have a negative serum pregnancy test at Screening (Visit 1) and a negative urine pregnancy test at Baseline (Visit 2).
- Females of non-childbearing potential must either be post-menopausal with spontaneous amenorrhea for at least 12 months or have undergone surgical sterilization.
- Subjects in good health as judged by the Investigator, based on medical history, physical examination, vital signs, serum chemistry labs, hematology values, and urinalysis.
- Subjects are considered reliable and capable of adhering to the Protocol and visit schedule according to the Investigator judgment.
Exclusion Criteria:
- Subjects who cannot discontinue treatment with therapies for the treatment of seborrheic dermatitis prior to the Baseline visit and during the study according to Excluded Medications and Treatments
- Planned excessive exposure of treated area(s) to either natural or artificial sunlight, tanning bed or other LED
- Subjects who cannot discontinue the use of strong P-450 cytochrome inhibitors e.g., indinavir, nelfinavir, ritonavir, clarithromycin, itraconazole, ketoconazole, nefazodone, saquinavir, suboxone and telithromycin for two weeks prior to the Baseline visit (Visit 2) and during the study
- Subjects who cannot discontinue the use of strong P-450 cytochrome inducers e.g., efavirenz, nevirapine, glucocorticoids, barbiturates (including phenobarbital), phenytoin, rifampin, and carbamazepine for two weeks prior to the Baseline visit (Visit 2) and during the study.
- Subjects with PHQ-8 >10 at Screening or Baseline visits.
- Previous treatment with ARQ-151 and ARQ-154.
- Subjects who have received oral roflumilast (Daliresp®, Daxas®) or other PDE-4 inhibitors (apremilast) within the past 4 weeks
- History of and/or concurrent condition of serious hypersensitivity (anaphylactic shock or anaphylactoid reaction) to PDE-4 inhibitors.
- Known allergies to excipients in ARQ-154 foam
-
Known or suspected:
- severe renal insufficiency or moderate to severe hepatic disorders
- hypersensitivity to component(s) of the investigational products
- history of severe depression, suicidal ideation
- Subjects with a history of a major surgery within 8 weeks prior to Baseline (Visit 2) or has a major surgery planned during the study
- Subjects with any condition on the treatment area which, in the opinion of the Investigator, could confound efficacy measurements.
- Subjects unable to apply product to the scalp due to physical limitations.
- Females who are pregnant, wishing to become pregnant during the study, or are breast-feeding.
- A clinically relevant history of abuse of alcohol or other drugs, at the discretion of the Investigator.
- Subjects who are unable to communicate, read or understand the local language, or who display another condition, which in the Investigator's opinion, makes them unsuitable for clinical study participation.
- Subjects who are family members of the clinical study site, clinical study staff, or sponsor, or family members of enrolled subjects.
- Any condition that in the Investigator's assessment would preclude the subject from participating in the study.
Information from the National Library of Medicine
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04091646
Contacts
| Contact: David Berk, MD | 805-418-5006 ext 5 | studyinquiry@arcutis.com |
Locations
Show 20 study locations
Sponsors and Collaborators
Arcutis Biotherapeutics, Inc.
| Responsible Party: | Arcutis Biotherapeutics, Inc. |
| ClinicalTrials.gov Identifier: | NCT04091646 |
| Other Study ID Numbers: |
ARQ-154-203 |
| First Posted: | September 17, 2019 Key Record Dates |
| Last Update Posted: | January 2, 2020 |
| Last Verified: | December 2019 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | Yes |
| Studies a U.S. FDA-regulated Device Product: | No |
Additional relevant MeSH terms:
|
Dermatitis Dermatitis, Seborrheic Skin Diseases |
Sebaceous Gland Diseases Skin Diseases, Eczematous Skin Diseases, Papulosquamous |