[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

How to apply

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Study’s contact

Call center

877‐277‐8566

Email address

IR-CTRegistration@allergan.com

Condition

Diabetes Mellitus,Gastroparesis

Treatment type

Interventional

Investigational product

Placebo

Phase

Phase 3

Sponsor

Allergan

ClinicalTrials.gov identifier

NCT03285308

Study number

RLM-MD-01

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About the study

This study will evaluate the safety and efficacy of Relamorelin compared to placebo in patients with diabetic gastroparesis. Patients will report daily severity scores of their diabetic gastroparesis symptoms.

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

Inclusion criteria
  1. Diagnosis of Type 1 or Type 2 diabetes mellitus
  2. Meet the per protocol criteria of diabetic gastroparesis
  3. Compliance with diary
  4. Compliance with the per protocol study treatment dosing instructions
Exclusion criteria
  1. Currently receiving nutrition intravenously, by nasogastric tube, or other feeding tube
  2. Actively experiencing anorexia nervosa, binge-eating, bulimia, or other eating disorder at the time of Screening (Visit 1)
  3. Diagnosis of Celiac Disease, also a history of non-celiac gluten sensitivity
  4. History of gastrointestinal disorders that may be similar to gastroparesis
  5. Functional dyspepsia diagnosed before the diagnosis of diabetes mellitus

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

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