Working…
COVID-19 is an emerging, rapidly evolving situation.
Get the latest public health information from CDC: https://www.coronavirus.gov.

Get the latest research information from NIH: https://www.nih.gov/coronavirus.
ClinicalTrials.gov
ClinicalTrials.gov Menu
Trial record 1 of 44 for:    Recruiting, Not yet recruiting, Active, not recruiting, Enrolling by invitation, Suspended Studies | Mallinckrodt
Previous Study | Return to List | Next Study

Impact of Acthar on Everyday Life of Participants With Severe Keratitis

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: NCT04169061
Recruitment Status : Recruiting
First Posted : November 19, 2019
Last Update Posted : August 3, 2020
Sponsor:
Information provided by (Responsible Party):
Mallinckrodt

Brief Summary:

We will need about 36 participants for this study.

Volunteers might be able to participate if:

  • they have bad noninfectious keratitis
  • early treatments failed or were not well accepted

Participants will be in the study for about 22 weeks:

  • 4 weeks for tests to see if the study might be good for them
  • 12 weeks of treatment with Acthar gel
  • 4 weeks to wean off Acthar gel and follow-up with the doctor

Condition or disease Intervention/treatment Phase
Keratitis Drug: Acthar Phase 4

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 36 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Multicenter, Open-label Study to Assess the Efficacy and Safety of Acthar® Gel in Subjects With Severe Keratitis
Actual Study Start Date : September 30, 2019
Estimated Primary Completion Date : August 31, 2020
Estimated Study Completion Date : August 31, 2020

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: All participants

Participants receive:

  • a shot of Acthar (80 units) under the skin twice a week for 12 weeks
  • a shot of Acthar (40 units) twice a week for 2 weeks
  • a shot of Acthar (40 units) once a week for 2 more weeks

At each visit they will have medical tests and answer questions about their symptoms.

Drug: Acthar
Acthar gel for subcutaneous injection
Other Name: Acthar Gel




Primary Outcome Measures :
  1. Responder scores on the IDEEL questionnaire [ Time Frame: within 88 days ]
    The Impact of Dry Eye on Everyday Life (IDEEL) questionnaire is made up of 57 questions divided into 3 sections. Each section is scored from 0 to 100; a higher score in the first two 2 sections means quality of life and treatment satisfaction got better, but a higher score in the third section means the symptoms of dry eye got more bothersome (so a lower score in that section is better). The highest possible score is 300, but the best possible score is 200.



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.


Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Has severe or recalcitrant keratitis
  • Did not respond to, or tolerate, treatment with topical cyclosporine or any immunosuppressant to treat keratitis
  • If able to reproduce, agrees to use 2 forms of effective contraception with a partner of the opposite sex for the duration of the study (through Visit 6)
  • Has normal eyelids, and protocol-defined physical and medical eye attributes
  • Agrees to avoid wearing contact lenses during the trial

Exclusion Criteria:

  • Is pregnant or breast-feeding
  • Is defined as vulnerable, or is employed by, or related to anyone involved in the study
  • Has a medical condition or history that might, per protocol or in the opinion of the investigator, compromise the participant's safety or study analysis

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): NCT04169061


Locations
Layout table for location information
United States, Arizona
Cornea and Cataract Consultants of Arizona Recruiting
Phoenix, Arizona, United States, 85032
Contact: Site Coordinator    602-258-4342    ccazresearch@aol.com   
United States, California
Global Research Management, Inc. Recruiting
Glendale, California, United States, 91204
Contact: Site Coordinator    818-246-2560    logi@lugeneeye.com   
Eye Research Foundation Active, not recruiting
Newport Beach, California, United States, 92663
United States, Kentucky
Eye Care Institute Recruiting
Louisville, Kentucky, United States, 40206
Contact: Site Coordinator    502-589-1500    kjohnson@eyecareinstitute.com   
United States, Massachusetts
Andover Eye Associates Recruiting
Raynham, Massachusetts, United States, 02767
Contact: Site Coordinator    978-685-8900    kkeohane@oraclinical.com   
United States, North Carolina
Vita Eye Clinic Recruiting
Shelby, North Carolina, United States, 28150
Contact: Site Coordinator    704-487-4099    annamhall91@gmail.com   
United States, Pennsylvania
Scott & Christie and Associates, PC Recruiting
Cranberry Township, Pennsylvania, United States, 06066
Contact: Site Coordinator    724-772-3000    nhindman@scottandchristie.com   
United States, Tennessee
Total Eye Care, P.A. Enrolling by invitation
Memphis, Tennessee, United States, 38119
Advancing Vision Research, LLC Recruiting
Nashville, Tennessee, United States, 37205
Contact: Site Coordinator    615-502-2871 ext 102    meganm@avrteam.com; brandiw@avrteam.com   
Sponsors and Collaborators
Mallinckrodt
Investigators
Layout table for investigator information
Study Director: Global Clinical Leader Mallinckrodt
Layout table for additonal information
Responsible Party: Mallinckrodt
ClinicalTrials.gov Identifier: NCT04169061    
Other Study ID Numbers: MNK14084113
First Posted: November 19, 2019    Key Record Dates
Last Update Posted: August 3, 2020
Last Verified: July 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
Keywords provided by Mallinckrodt:
Severe or recalcitrant keratitis
Additional relevant MeSH terms:
Layout table for MeSH terms
Keratitis
Corneal Diseases
Eye Diseases
Adrenocorticotropic Hormone
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs