Baricitinib for Cutaneous Dermatomyositis

Dermatomyositis Clinical Trial

Official title:

An Open-Label Pilot Study to Evaluate the Efficacy and Safety of Baricitinib in Subjects With Cutaneous Dermatomyositis

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT05361109
• Other study ID #: STUDY00014444
• Secondary ID: CUDM001
• Status: Withdrawn
• Phase: Phase 2
• Start date: June 1, 2022
• Est. completion date: March 31, 2023

Study information

• Verified date: August 2023
• Source: University of Washington
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase 2, single-center study in patients with active cutaneous DM who have had an inadequate response. An inadequate response is defined as no improvement with standard of care treatment based on the investigator's opinion.

All subjects will initially receive baricitinib 2mg daily for 8 weeks. If no unexpected serious adverse events related to baricitinib have occurred during the first 8 weeks of treatment in the opinion of the investigator, the dose will be increased to 4 mg daily for 16 weeks. Visits are scheduled at baseline, 4 weeks, 8 weeks, 12 weeks, 16 weeks, 20 weeks, and 24 weeks. Evaluation of primary endpoint occurs at week 24. All subjects receive a phone call from study

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: March 31, 2023
• Est. primary completion date: March 31, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Male or non-pregnant, non-nursing female

2. Age =18 years at time of consent

3. Typical cutaneous DM manifestations including heliotrope rash, Gottron's papules/sign, V-sign, shawl sign, holster sign, confirmed by skin biopsy, with or without DM muscle disease classified based on the Bohan and Peter criteria at screening and baseline visit

4. Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI) activity score = 12 corresponding to moderate to severe disease activity at screening and baseline visit

5. Active disease (i.e., CDASI = 12) despite adequate prior treatment experience with corticosteroids, immunosuppressants, or biologics

6. Patients taking methotrexate must be on a stable dose for at least 4 weeks prior to baricitinib initiation

7. Patients who have received mycophenolate, azathioprine, cyclosporine, or tacrolimus must have discontinued for at least 4 weeks prior to signing the informed consent.

8. Patients who have received IVIG, rituximab or any other biologic agents must have discontinued for at least 6 months prior to signing the informed consent

9. Patients taking oral corticosteroids, the dose must be = 15 mg/day prednisone or equivalent and not be changed for 2 weeks prior to baseline visit

10. Females of childbearing potential and males with female partners of childbearing potential may participate in this study only if using a highly effective method of contraception

Highly Effective Methods of Contraception:

1. A tubal ligation, or surgical sterilization

2. FDA approved hormonal contraceptive such as oral contraceptives, emergency contraception used as directed, patches, implants, injections, rings, or hormonally impregnated intrauterine device (IUD)

3. Intrauterine device (IUD)

4. Abstinence if this method of contraception coincides with normal lifestyle choice of the participant. Abstinence for the duration of the study is not an acceptable method of contraception for the purposes of this study.

Exclusion Criteria:

1. Previous treatment with baricitinib.

2. Previous treatment with tofacitinib or updacitinib.

3. Current use of strong Organic Anion Transporters 3 (OAT3) inhibitors including probenecid.

4. Uncontrolled or rapidly progressive myositis or interstitial lung disease at the discretion of the investigator which is likely to warrant escalation in therapy beyond permitted background medications.

5. Cancer-associated myositis (myositis diagnosed within 2 years of a diagnosis of cancer).

6. Patients who are known to be positive for the anti-TIF1-? (p155/140) or anti-NXP2 autoantibody unless they are determined not to be associated with malignancy at the discretion of the investigator.

7. Other inflammatory diseases that might confound the evaluations of efficacy including but not limited to rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), psoriatic arthritis, inflammatory bowel disease.

8. Recurrent or chronic bacterial, viral, fungal, mycobacterial, or other infections including HIV, Hepatitis B or C, latent TB (TB not adequately treated according to guidelines)

9. History of recurrent herpes zoster, disseminated (multi-dermatomal) herpes zoster, disseminated herpes simplex or ophthalmic zoster. Herpes zoster lesions within 90 days prior to screening.

10. Primary or secondary immunodeficiency.

11. Current uncontrolled renal, gastrointestinal, endocrine, pulmonary, cardiac, or neurologic disease, which, in the opinion of the investigator, might place the patient at unacceptable risk for participation in this study.

12. History of malignancy within 5 years prior to screening, except for appropriately treated carcinoma in situ of the cervix and non-melanoma skin carcinoma.

13. History of lymphoproliferative disease, including lymphoma, and monoclonal gammopathy of undetermined significance.

14. History of venous thromboembolism, including deep vein thrombosis and pulmonary embolism.

15. History of alcohol, drug, or chemical abuse within one year prior to signing the informed consent form.

16. Laboratory exclusion criteria within 60 days of Consent including

• Hemoglobin (Hgb) < 8g/dL

• White Blood Count (WBC) < 3,000/µL fidential Page 13 of 40

• Absolute Neutrophil Count (ANC) < 1,500/µL

• Absolute Lymphocyte Count (ALC) < 800/µL

• Platelets < 100,000/µL

• eGFR < 60 ml/min

• ALT or AST >1.5 times ULN not due to DM.

17. Major surgery within 8 weeks prior to Screening or planned major surgery at any time during participation in the study.

18. Immunization with a live/attenuated vaccine within 4 weeks prior to Screening.

19. Pregnant or nursing women, or women of child-bearing potential who plan to become pregnant prior to 14 weeks after the last dose of baricitinib treatment.

20. Patients of reproductive potential not willing to use a highly effective method of contraception as defined in Section 5.3.1.10.

21. Prisoners, or subjects who are compulsory detained, or cannot provide informed consent without the use of a legally authorized representative (LAR).

Related Conditions & MeSH terms

• Dermatomyositis

Intervention

Drug:
• Baricitinib
The investigational medicinal product (IP) for this study is baricitinib 2mg. The dose will be administered as one 2mg tablet by mouth once daily for the first 8 weeks of study. If no unexpected serious adverse events related to baricitinib in the opinion of the investigator occur during the first 8 weeks of treatment, the dose will be increased to two 2mg tablets (4mg daily) for the remaining 16 weeks of study. All study participants will take baricitinib in combination with standard of care background therapy.

Locations

Country	Name	City	State
United States	University of Washington Medical Center	Seattle	Washington

Sponsors (1)

Lead Sponsor	Collaborator
University of Washington

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cutaneous Disease Activity Severity Index (CDASI) activity score	Change in Cutaneous Disease Activity Severity Index (CDASI) activity score (0-100), higher scores mean a worse outcome	24 Weeks
Secondary	Cutaneous Disease Activity Severity Index (CDASI) activity score	Change in Cutaneous Disease Activity Severity Index (CDASI) activity score (0-100), higher scores mean a worse outcome	12 weeks
Secondary	International Myositis Assessment & Clinical Studies Group (IMACS) Disease Activity Core Set Measures	Change in International Myositis Assessment & Clinical Studies Group (IMACS) Disease Activity Core Set Measures	12 weeks and 24 weeks
Secondary	SF-36	Change in SF-36	12 weeks and 24 weeks
Secondary	Dermatology Life Quality Index (DLQI)	Change in Dermatology Life Quality Index (DLQI)	12 weeks and 24 weeks
Secondary	Adverse event	Adverse event monitoring	24 weeks