Phase 1Completed

Evaluation of Patient Performance Using the Metoject Device for Subcutaneous Injection in Rheumatoid Arthritis (RA)Patient

Evaluation of Rheumatoid Arthritis Patient Performance Using the Metoject® Prefilled Pen (Methotrexate 50 mg/mL, Prefilled Pen) for Subcutaneous Injection and Subsequent Pharmacokinetic Assessment of Drug Delivery

Sponsor
medac GmbH (Industry)
Enrolment
105 enrolled
Conditions
Rheumatoid Arthritis (RA)
Interventions
Methotrexate (Metoject® prefilled pen)
Ages
children, adults, older adults
Registry
NCT01871961

Full record on ClinicalTrials.gov

From the registry

To evaluate the human factors/usability of Rheumatoid Arthritis (RA) patients with the Metoject® prefilled pen (including a label comprehension assessment and a device robustness evaluation).

Primary outcomes

  • To evaluate the human factors/usability of Rheumatoid Arthritis (RA) patients with the Metoject® prefilled pen (including a label comprehension assessment and a device robustness evaluation).

History

  1. Last registry update

  2. Registered

  3. Study completion

  4. Primary completion

  5. Started