Efficacy and Safety of H.P. ACTHAR GEL in Adults With Retinal Vasculitis

NCT03066869 | Unknown Phase 4 FDA Drug

• 1 other identifier: 120160924
• Study Type: interventional
• Target: 40
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to evaluate the short- and long-term efficacy and safety of Acthar for the treatment of adults with non-infectious retinal vasculitis.

Conditions

Uveitis, Posterior; Vasculitis Retinal

Outcome Measures

Primary Outcomes (1)

• Percentage of responders to Acthar at the end of treatment.

  A responder will be defined by the binominal presence or absence of active retinal vasculitis as evaluated at Week 24. Active retinal vasculitis is defined as angiographic leakage from retinal arterioles, venules, or capillaries as determined by investigator, seen on wide-field angiography. Complete resolution or absence of active retinal vasculitis at Week 24 is considered success or "remission".

  24 Weeks

Secondary Outcomes (3)

• Presence or absence of active retinal vasculitis at all other time points.

  1 Day to 24 Weeks

• Safety assessments, including drug tolerability and adverse events; other ocular and/or systemic complications.

  1 Day to 24 Weeks

• Percentage of patients requiring rescue therapy.

  1 Day to 24 Weeks

Study Arms (1)

H.P. ACTHAR GEL

EXPERIMENTAL

Drug: H.P. ACTHAR GEL

Interventions

H.P. ACTHAR GEL DRUG

H.P. Acthar Gel is an adrenocorticotropic hormone (ACTH) analogue indicated for ophthalmic diseases.

H.P. ACTHAR GEL

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Any adult patient with active retinal vasculitis (involving arteries or veins) as a manifestation of non-infectious ocular inflammatory disease; fundus must be viewable with wide-field FA in the study eye
• Patients already on non-steroidal immunosuppressive therapy may continue on this during the study, but the dose must not be increased or decreased within 6 weeks of initiating the trial
• Willing and able to sign the informed consent form

You may not qualify if:

• Patients under age 18
• Patients who are pregnant (must be ruled out in women of child-bearing age)
• Active infectious ocular or systemic disease
• Patients with active infectious ocular or extraocular disease
• Patients with history of malignancy, except for dermatologic entities of basal or squamous cell carcinoma which have been completely excised or removed previously
• Patients with systemic illness involving abnormalities of the hypothalamic-pituitary-adrenal axis; patients with primary adrenocortical insufficiency or adrenocortical hyperfunction
• Patients with known hypersensitivity to Acthar
• Patients on other non-steroidal systemic immunomodulatory medications with dose adjusted sooner than 6 weeks prior to study drug administration
• Patients currently on or recently treated with (within 6 weeks) systemic corticosteroid
• Patients with periocular or intraocular injections of medications administered to help control inflammation sooner than 6 weeks prior to study drug administration
• Patients with severe disease that warrants critical attention, deemed unsafe for the study by the investigator, or contraindicated, including but not limited to, patients with scleroderma, osteoporosis, systemic fungal infections, ocular herpes simplex, recent surgery, history of or the presence of a peptic ulcer, congestive heart failure, uncontrolled hypertension, or sensitivity to proteins of porcine origin. Administration of live or live attenuated vaccines is contraindicated in patients during the entire duration of the study and for one month prior

Sponsors & Collaborators

• Ocular Immunology and Uveitis Foundation: lead

Study Sites (1)

Ocular Immunology & Uveitis Foundation

Waltham, Massachusetts, 02451, United States

RECRUITING

MeSH Terms

Conditions

Uveitis, Posterior; Retinal Vasculitis

Condition Hierarchy (Ancestors)

Panuveitis; Uveitis; Uveal Diseases; Eye Diseases; Retinal Diseases; Vasculitis; Vascular Diseases; Cardiovascular Diseases

Central Study Contacts

C. Stephen Foster, MD

CONTACT

781-891-6377; sfoster@mersi.com

Study Design

• Study Type: interventional
• Phase: phase 4
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 30, 2016
• First Posted: March 1, 2017
• Study Start: March 22, 2017
• Primary Completion: February 1, 2020
• Study Completion: August 1, 2020
• Last Updated: September 12, 2019

Record last verified: 2019-09

Locations

US (1)