Study of TDM-180935 in Atopic Dermatitis Patients

Atopic Dermatitis Clinical Trial

Official title:

A Randomized, Vehicle-Controlled, Parallel Group Study of Topical TDM-180935 to Evaluate the Preliminary Efficacy, Safety, Tolerability, and Pharmacokinetics in Atopic Dermatitis Patients

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06363461
• Other study ID #: 239-13851-202
• Status: Recruiting
• Phase: Phase 2
• Start date: April 13, 2024
• Est. completion date: October 31, 2024

Study information

• Verified date: April 2024
• Source: Technoderma Medicines Inc.
• Contact: Arthur P. Bertolino, MD, PhD, MBA
• Phone: +1 6169281145
• Email: arthur.bertolino[@]innovationderm.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Randomized, Vehicle-controlled, Parallel Group Study of TDM-180935 in Atopic Dermatitis Patients

Description:

Protocol 239-13851-202 is a Phase 2a study entitled "A Randomized, Vehicle-Controlled, Parallel Group Study of Topical TDM-180935 to Evaluate the Preliminary Efficacy, Safety, Tolerability, and Pharmacokinetics in Atopic Dermatitis Patients". Eligible subjects (24) in the randomized portion of the study will be randomized (2:2:1:1) to 1 of the 4 groups (low dose vs high dose vs placebo 1 vs placebo 2) and treated for 8 weeks. Eligible subjects (6) in the PK (pharmacokinetics) cohort will be treated with the high dose in an open label fashion.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 24
• Est. completion date: October 31, 2024
• Est. primary completion date: September 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. A) Patient is a male = 18 years old at Visit 1/Screening. B) Patient is a post-menopausal or surgically sterile female = 18 years old at Visit 1/Screening.

2. Patient has provided written informed consent.

3. Male patients who are sexually active with a female partner and are not surgically sterile must use a highly effective method of birth control as described in the informed consent form. Note: Male patients must refrain from sperm donation for at least 90 days after application of their last dose of IP (investigational product).

4. Patient has active mild or moderate AD with a modified-Eczema Area and Severity Index (m-EASI) score of 5-16 and a history of AD duration = 2 years.

5. Patient has an AD body surface area (BSA) between 3 and 12% in the area to be treated (excluding head/neck, hands/feet, genitalia, and intertriginous areas) at Baseline.

6. Patient is willing and able to apply the IP(s) as directed, comply with study instructions (including avoiding direct sunlight exposure to the areas of IP application), and commit to all follow-up visits for the duration of the study. Note: The use of topical sunscreen is permitted provided the patient has used the sunscreen previously and it does not contain any prohibited medications/ingredients.

7. Patient, in the investigator's opinion, is in good general health and free of any disease state or physical condition that might impair evaluation or exposes the patient to an unacceptable risk by study participation.

8. Patient agrees to apply a bland moisturizer as directed for the duration of the study.

9. Patient has normal renal and hepatic function as determined by the Visit 1/Screening laboratory results in the opinion of the investigator.

10. [For PK Cohort Only] Patient is a non-smoker, defined as not having smoked or used any form of tobacco or non-tobacco products containing nicotine in more than 6 months before Visit 2/Baseline.

11. [For PK Cohort Only] Patient has a body mass index (BMI) of 19 to 32 kg/m2 inclusive and body weight not less than 50 kg at Visit 1/Screening.

Exclusion Criteria:

1. Patient has any dermatological disorders of the skin within 20 cm of the areas to be treated with the possibility of interfering with the application of the IP or examination method, such as fungal or bacterial infections, psoriasis, folliculitis, notable scarring (linear scar > 2.5 cm, etc.), or skin atrophy at Visit 2/Baseline.

2. Patient has any skin pathology or condition that, in the investigator's opinion, could interfere with the evaluation of the IP or requires use of interfering topical, systemic, or surgical therapy at Visit 2/Baseline.

3. Patient has any visible inflammatory skin disease, injury, or condition of their skin that could compromise patient safety and/or interfere with the evaluation of local or systemic assessments performed during the study.

4. Patient has a known or suspected malignancy at Visit 2/Baseline excluding basal cell skin cancer unless it is associated with the area to be treated per Exclusion Criterion no. 1.

5. Patient has a positive blood screen for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C antibody.

6. Patient has any condition, which, in the investigator's opinion, would make it unsafe for the patient to participate in this study, including clinically significant abnormal laboratory, or 12-lead electrocardiogram (ECG) findings during the screening period or Visit 2/Baseline prior to dosing of the IP.

7. Patient has a hospital admission or major surgery within 30 days prior to Visit 2/ Baseline or planned for during the study.

8. Patient is currently enrolled in an investigational drug, biologic, or device study.

9. Patient has used an investigational drug, investigational biologic, or investigational device treatment within 30 days or 5 half-lives, whichever is longer, prior to Visit 2/Baseline.

10. Patient has a history of prescription drug abuse, or illicit drug use within 6 months prior to Visit 1/Screening.

11. Patient has a history of alcohol abuse according to medical history within 6 months prior to Visit 1/Screening.

12. Patient has a positive screen for alcohol or drugs of abuse at Visit 1/Screening or Visit 2/Baseline. Note: Patients with a positive drug screen believed by the investigator to be the result of medically appropriate prescription medication use can be enrolled with Medical Monitor approval.

13. Patient has used topical cosmetic (excluding bland moisturizers), herbal, over-the- counter (OTC) or prescription products within areas to be treated within 2 weeks prior to dosing at Visit 2/Baseline.

14. Patient has used systemic prescription treatment for AD or that in the opinion of the investigator may affect the patient's AD (examples include, but are not limited to PDE4 (Phosphodiesterase-4) inhibitors, corticosteroids, immunomodulators, antimetabolites, antibiotics, retinoids, etc.) within 4 weeks prior to Visit 2/Baseline. Note: systemic corticosteroids do not include intranasal, inhaled, or ophthalmic corticosteroids for the management of allergies, pulmonary disorders, or other conditions.

15. Patient has used systemic biologic therapy (i.e., dupilumab) for AD or that in the opinion of the investigator may affect the patient's AD within 5 half-lives of the biologic therapy prior to Visit 2/Baseline.

16. Patient has been diagnosed with COVID-19 (Coronavirus Disease of 2019) within 4 weeks of Visit 1/Screening.

17. Patient is unable to communicate or cooperate with the investigator due to language problems, poor mental development, or impaired cerebral function.

18. Patient has previously been treated with the IP.

19. Patient has a history of sensitivity to any of the ingredients in the IP.

20. Patient has ongoing or recent history of any other uncontrolled and/or clinically significant systemic disease or condition which, in the investigator's opinion, should exclude participation in the study.

21. [For PK Cohort Only] Patient has a donation or blood collection of more than 1 unit (approximately 450 mL) of blood (or blood products) or acute loss of blood during the 90 days prior to Visit 2/Baseline.

22. [For PK Cohort Only] Patient has used systemic prescription medications, herbal (including St John's Wort, herbal teas and garlic extracts) supplements within 14 days prior to dosing at Visit 2/Baseline.

23. [For PK Cohort Only] Patient has used systemic OTC medications or vitamins within 7 days prior to dosing at Visit 2/Baseline. (Note: Use of acetaminophen at < 3g/day is permitted).

24. [For PK Cohort Only] Patient received a live or live attenuated vaccine within 4 weeks of dosing at Visit 2/Baseline.

Related Conditions & MeSH terms

• Atopic Dermatitis
• Dermatitis
• Dermatitis, Atopic
• Eczema

Intervention

Drug:
• TDM-180935 topical ointment 1.0%
Eligible patients in the randomized portion of the study will be randomized (2:2:1:1) to 1 of the 4 groups. The assigned drug will be applied once daily for 8 weeks, with application to the active lesions excluding head/neck, hands/feet, genitalia, and intertriginous areas.
• TDM-180935 topical ointment 2.0%
Eligible patients in the randomized portion of the study will be randomized (2:2:1:1) to 1 of the 4 groups. The assigned drug will be applied once daily for 8 weeks, with application to the active lesions excluding head/neck, hands/feet, genitalia, and intertriginous areas.
• TDM-180935 topical vehicle ointment 1
Eligible patients in the randomized portion of the study will be randomized (2:2:1:1) to 1 of the 4 groups. The assigned placebo will be applied once daily for 8 weeks, with application to the active lesions excluding head/neck, hands/feet, genitalia, and intertriginous areas.
• TDM-180935 topical vehicle ointment 2
Eligible patients in the randomized portion of the study will be randomized (2:2:1:1) to 1 of the 4 groups. The assigned placebo will be applied once daily for 8 weeks, with application to the active lesions excluding head/neck, hands/feet, genitalia, and intertriginous areas.

Locations

Country	Name	City	State
United States	Site 7	Anderson	South Carolina
United States	Site 3	Austin	Texas
United States	Site 1	College Station	Texas
United States	Site 8	Covington	Louisiana
United States	Site 4	New Brighton	Minnesota
United States	Site 2	Norfolk	Virginia
United States	Site 5	Rolling Meadows	Illinois

Sponsors (2)

Lead Sponsor	Collaborator
Technoderma Medicines Inc.	Therapeutics, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Incidence (severity and causality) of any local and systemic AEs (adverse events)	Collection of adverse events	8 weeks
Other	Number of patients with presence (and severity) of the following LSRs (local skin reactions): skin pigmentation (hyperpigmentation and hypopigmentation), edema, erosion,scaling, and burning/stinging	Collection of LSRs at weeks 2, 4, 6, and 8	8 weeks
Other	Changes from Baseline in vital signs (temperature)	Collection of temperature at weeks 4 and 8	8 weeks
Other	Changes from Baseline in vital signs (systolic and diastolic blood pressure)	Collection of systolic and diastolic blood pressure at weeks 4 and 8	8 weeks
Other	Changes from Baseline in vital signs (heart rate)	Collection of heart rate at weeks 4 and 8	8 weeks
Other	Changes from Baseline in vital signs (respiration rate)	Collection of respiration rate at weeks 4 and 8	8 weeks
Other	Changes from baseline in clinical laboratory tests (including Blood Chemistries, Hematology, and Urinalysis)	Collection of safety lab results at weeks 4 and 8	8 weeks
Other	Number of participants with abnormal ECG readings	Collection of ECGs at day1, week 4 and week 8	8 weeks
Primary	Change in m-EASI (modified Eczema Area and Severity Index) score	Collection of EASI (Eczema Area and Severity Index) results at week 8. The total m-EASI score may range from zero (0) to a maximum of 64.8, and higher scores mean a worse outcome.	8 weeks
Secondary	Proportion of patients with a = 2 point improvement in vIGA-AD score (validated Investigator's Global Assessment for Atopic Dermatitis score)	Collection of vIGA-AD score (validated Investigator's Global Assessment for Atopic Dermatitis score) at week 8. The vIGA-AD is a static morphological 5-point ordinal scale from 0 (clear) to 4 (severe).	8 weeks
Secondary	Change in m-EASI (modified Eczema Area and Severity Index) score	Collection of EASI (Eczema Area and Severity Index) results at weeks 2, 4, and 6. The total m-EASI score may range from zero (0) to a maximum of 64.8, and higher scores mean a worse outcome.	6 weeks
Secondary	Proportion of patients with a 50% improvement in m-EASI (modified Eczema Area and Severity Index) score	Collection of EASI (Eczema Area and Severity Index) results at week 8. The total m-EASI score may range from zero (0) to a maximum of 64.8, and higher scores mean a worse outcome.	8 weeks
Secondary	Proportion of patients with a 75% improvement in m-EASI (modified Eczema Area and Severity Index) score	Collection of EASI (Eczema Area and Severity Index) results at week 8. The total m-EASI score may range from zero (0) to a maximum of 64.8, and higher scores mean a worse outcome.	8 weeks
Secondary	Proportion of patients with a 90% improvement in m-EASI (modified Eczema Area and Severity Index) score	Collection of EASI (Eczema Area and Severity Index) results at week 8. The total m-EASI score may range from zero (0) to a maximum of 64.8, and higher scores mean a worse outcome.	8 weeks
Secondary	Change in BSA (body surface area) affected	Collection of BSA affected at weeks 2, 4, 6, and 8	8 weeks
Secondary	Proportion of patients with a 4-point improvement from Baseline in WI-NRS (Worst Itch-Numeric Rating Scale) score	Collection of WI-NRS (Worst Itch-Numeric Rating Scale) score at week 8. The level of itching is described on an 11-point scale anchored at 0, representing "no itch" and 10, representing, "worst itch imaginable".	8 weeks