Bioavailability in Patient With Psoriasis: Metoject Prefilled Pen
Completed · Phase 1
Conditions studied: Psoriasis
In brief
This study is conducted to assess the relative bioavailability of MTX administered subcutaneously via a prefilled pen (50mg/mL) compared with MTX administered via IM injection (25mg/mL).
Key facts
- Study ID
- NCT02097173
- Run by
- medac GmbH
- People needed
- 35
- Starts
- 2013-05-01
- Last updated by the study team
- 2015-03-17
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Is able to understand and follow instructions during the study
- Has a diagnosis of moderate to severe psoriasis based on a dermatologic evaluation
- Provides written informed consent
- Is male or female and is aged 18 to 65 years, inclusive
- Has a body mass index (BMI) within the range 18 through 30 kg/m2.
- Main Exclusion Criteria:
- Is receiving concomitant treatment for psoriasis with a biologic or conventional systemic treatments (eg, cyclosporine, azathioprine, fumaric acid esters, Leflunomide), other than MTX every week
- Has used antibiotics within 14 days prior to Screening or requires use prior to study completion
- Has used any of the following medications within 14 days prior to Screening or requires use prior to study completion, unless on a stable, daily dose: Non steroidal antiinflammatory drugs (NSAIDs), Diuretics, Folic Acid, Hydrochloroquine, Probenicid, Proton-pump inhibitors
- Has, other than psoriasis, any uncontrolled cardiac disease, liver disease, lung disease, hematologic disease, gastrointestinal disease, or other systemic disease, that in the opinion of the investigator, would present an unacceptable risk if he or she were to participate in the study
- Has ongoing acute or chronic infection within 14 days prior to Screening
- Has renal insufficiency , hepatic insufficiency, impaired hematopoiesis, known severe, acute, or chronic infection, history of malignancy, history of or suspected abuse of drugs or alcohol
- allergic reactions or serious adverse reactions to the study drug
- Is a female subject who is pregnant, trying to become pregnant, or breast feeding, or of childbearing potential, sexually active and not practicing a highly reliable method of birth control
- Is a male subject with a female partner of childbearing potential, not had a vasectomy and not using a condom and/or cervical cap/diaphragm with spermicide
Where it is running
- Clinical Trials of Texas, Inc. — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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