Protocol for H.P. Acthar Gel in Moderately to Severely Active Psoriatic Arthritis
The recruitment status of this study is unknown because the information has not been verified recently.
Verified September 2013 by Fiechtner, Justus J., M.D., P.C..
Recruitment status was Recruiting
Information provided by (Responsible Party):
Fiechtner, Justus J., M.D., P.C.
First received: September 3, 2013
Last updated: September 9, 2013
Last verified: September 2013
Psoriatic arthritis is a heterogeneous chronic inflammatory disorder involving joints, tendon sheaths, entheses, and the axial skeleton as well as skin and nails. This is an open-label trial with H.P. Acthar Gel (80 units/1mL) Subcutaneous injection administered twice weekly. To evaluate the signs and symptoms of psoriatic arthritis after 12 weeks, including American College of Rheumatology 20,Clinical Disease Activity Index, Disease Activity Index 28, Dactylitis and adverse events.
Drug: Open label H.P. Acthar Gel
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
||Title of Study: A Single-Site, Investigator Initiated Open-Label Trial of H.P. Acthar Gel (Repository Corticotropin Injection) an Adrenocorticotropic Hormone (ACTH) Analogue in Subjects With Moderately to Severely Active Psoriatic Arthritis (PsA)
Primary Outcome Measures:
- ACR20 (American College of Rheumatology 20) [ Time Frame: Week 12 ] [ Designated as safety issue: No ]
To evaluate the efficacy of H.P. Acthar Gel given subcutaneously twice weekly on the signs and symptoms of psoriatic arthritis after 12 weeks of administration.
ACR20 (American College of Rheumatology 20) at week 12
Secondary Outcome Measures:
| Estimated Enrollment:
| Study Start Date:
| Estimated Study Completion Date:
| Estimated Primary Completion Date:
||July 2014 (Final data collection date for primary outcome measure)
Experimental: H.P. Acthar Gel SQ injection
Open-label H.P. Acthar Gel 80 units subcutaneously twice weekly for 12 weeks with a 12 week extension.
Drug: Open label H.P. Acthar Gel
Open-label H.P. Acthar Gel 80 units given subcutaneously twice weekly for 12 weeks with 12 week extension.
Other Name: ACTH
The subjects in this study will be adult men and women ages 18-75 years of age at the time of screening with chronic, moderately-to-severely active PsA and meeting ACR criteria.
|Ages Eligible for Study:
||18 Years to 75 Years
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
- In the opinion of the investigator, must have adequate reading and writing abilities (in their native language) such that the subject can comprehend and complete the informed consent, and all protocol-related assessments.
- Age 18-75 years at the time of screening
- Written informed consent and any locally required authorization (e.g. HIPAA) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations.
- Subject has had a diagnosis of psoriatic arthritis (by the Classification of Psoriatic Arthritis (CASPAR) criteria) for at least 6 months.
- Subject must have > 6 tender and >6 swollen joint count at screening.
- Subject must have > 30 minutes of morning joint stiffness.
- For subjects receiving non-steroidal anti-inflammatory drugs (NSAIDs) (including PRN use): the subject must be on stable dose for >4 weeks prior to initiation of H.P. Acthar Gel.
- For subjects receiving any Disease-Modifying Anti-Rheumatic Drug (DMARD) or Biologic agent: subject has received treatment for >8 weeks, with a stable does for > 4 weeks prior to initiation of H.P. Acthar Gel.
- For subjects receiving oral corticosteroids: the subject must be on a stable dose (not to exceed the equivalent of 10mg of prednisone per day) for >2 weeks prior to initiation of H.P. Acthar Gel.
Subject has a negative test for tuberculosis within 6 months before initiating H.P. Acthar Gel defined as either:
- Negative purified protein derivative (PPD)
- Negative Quantiferon test, or
- Negative chest x-ray
Females of childbearing potential must use an effective method of birth control and avoid pregnancy from screening through 60 days after final dose of H.P. Acthar Gel unless surgically sterile (i.e. bilateral tubal ligation, bilateral oophorectomy, or complete hysterectomy), has a sterile male partner, is >1 year postmenopausal or practices abstinence (not have sexual intercourse):
- Subject has a planned surgical intervention between baseline and the week 24 evaluation.
- Subject has any concurrent medical condition or uncontrolled, clinically significant systemic disease (eg, renal failure, congestive heart failure, uncontrolled hypertension, primary adrenocortical insufficiency or adrenocortical hyperfunction, peptic ulcer or sensitivity to proteins of porcine origin)
- Subject has a diagnosis of scleroderma, osteoporosis, fungal infections or ocular herpes simplex
- History of any type of malignancy <5 years before enrollment into the study (apart from basal cell carcinoma)
- Any live or attenuated vaccine within 4 weeks prior to signing the informed consent form (administration of killed vaccines is acceptable)
- Subject has active tuberculosis
- Any know history of allergy or reaction to any component of H.P. Acthar Gel
- Known history of a primary immunodeficiency or an underlying condition such as human immunodeficiency virus (HIV) infection.
- Employees of the clinical study site or any other individuals involved with the conduct of the study or immediate family members of such individuals
- Concurrent enrollment in any other clinical study with an investigational product within 4 weeks prior to enrollment into the study.
Lactating or pregnant females or females who intend to become pregnant anytime from initiation of screening through 60 days post last dose of H.P. Acthar Gel
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, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01939132
|Justus J. Fiechtner, MD, PC
|Lansing, Michigan, United States, 48910 |
|Contact: Tresa Montroy 517-272-9727 ext 24 firstname.lastname@example.org |
|Contact: Amanda Hutchins 517-272-9727 ext 24 email@example.com |
|Principal Investigator: Justus J Fiechtner, MD, MPH |
Fiechtner, Justus J., M.D., P.C.
||Fiechtner, Justus J., M.D., P.C.
History of Changes
|Other Study ID Numbers:
|Study First Received:
||September 3, 2013
||September 9, 2013
||United States: Food and Drug Administration
Keywords provided by Fiechtner, Justus J., M.D., P.C.:
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on May 26, 2016
Skin Diseases, Papulosquamous
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs