Open Label Safety Study of Tradipitant in Idiopathic and Diabetic Gastroparesis

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-70
SponsorVanda Pharmaceuticals

About this trial

This is a multicenter, open label, 3-month safety study with tradipitant in patients with idiopathic and diabetic gastroparesis.

Eligibility criteria

Qualifiers

Diagnosed with gastroparesis

Demonstrated delayed gastric emptying

Presence of moderate to severe nausea

Body Mass Index (BMI) of ≥18 and ≤40 kg/m2

Disqualifiers

Another active disorder or treatment which could explain or contribute to symptoms of gastroparesis

A positive test for drugs of abuse at the screening or evaluation visits

Pregnancy or nursing

Evidence of uncontrolled blood glucose (including HbA1C >11% at screening or metabolic crisis in past 60 days)

Trial design

Treatments tested in this trial

  • Tradipitant

Treatment groups

100 Participants
are divided into 1 treatment group

Sponsors and collaborators