Title
A First Time in Human Study in Healthy Volunteers and Patients
A Four Part, Phase 1, First Time in Human, Single Centre Study in Healthy Male Subjects, Patient Volunteers With Crohn's Disease and in Healthy Patient Volunteers With a Terminal Ileostomy
Phase
Phase 1Lead Sponsor
VHsquared Ltd.Study Type
InterventionalStatus
Completed No Results PostedIndication/Condition
Crohn's DiseaseIntervention/Treatment
v565 ...Study Participants
47A multi-part study to investigate the safety, tolerability and local and systemic pharmacokinetics of V565
single ascending dose of V565
Multiple dose
Single and multiple dose
Open-label single dose
Open-label single ascending dose
Oral placebo single dose (Part 1) or TID for 14 days (Part 2)
Inclusion Criteria: Parts 1 and 2 Adult male subjects aged 18 to 45 years inclusive. Body mass index (BMI) between 18.0 and 32.0 kg/m2 inclusive. Body weight between 50.0 and 100.0 kg inclusive. Subjects who are healthy as determined by pre study medical history, physical examination and 12-lead ECG, and clinical laboratory tests Part 3 Adult male or female subjects aged 18 to 65 years. Ileostomy for a minimum of 18 months for a non malignant disease indication. A BMI between 18.0 and 32.0 kg/m2 inclusive. Body weight between 50.0 and 100.0 kg inclusive. Subjects who are healthy as determined by pre study medical history, physical examination and 12-lead ECG, and clinical laboratory tests Part 4 Adult male or female subjects aged 18 to 65 years. A confirmed diagnosis of Crohn's disease for a minimum of 6 months. A BMI between 15.0 and 32.0 kg/m2 inclusive. Subjects who have no other significant co-morbidity (other than those associated with Crohn's disease). Subjects whose medical history, physical examination, clinical laboratory test results and 12-lead ECG have no clinically relevant abnormalities (other than those associated with Crohn's disease). Exclusion Criteria: Parts 1 and 2 A clinically significant abnormal medical history or clinically significant abnormal physical examination, including history of febrile illness within 1 week prior to the first dose. A history of severe allergies, non-allergic drug reactions, or multiple drug allergies. A known hypersensitivity to TNF inhibitors or any of the inactive ingredients of the study treatment. A history of significant gastrointestinal (GI) disease, including GI motility disorders, GI malignancy or of polyposis coli. Previous surgery to the GI tract with the exception of appendectomy. A history of malignancy. Any other condition which in the investigator's opinion will interfere with the trial or interpretation of the results. Part 3 A history of Crohn's disease. A clinically significant abnormal medical history (other than the condition leading to ileostomy) or clinically significant abnormal physical examination, including history of febrile illness within 1 week prior to the first dose. A history of severe allergies, non-allergic drug reactions, or multiple drug allergies. A known hypersensitivity or contraindication to TNF inhibitors or any of the inactive ingredients of the study treatment. A known history of heart disease. Any clinical evidence of active inflammatory bowel disease. Any other condition which in the investigator's opinion will interfere with the trial or interpretation of the results. Part 4 Subjects with severe Crohn's disease such as: those requiring surgery; those with a current abscess; those with a non inflammatory stricture; those with a history of obstruction. Having ever received anti-TNF-α therapy or other biologics. Required an increase in dose of either steroids or immunosuppressant therapy within the past 6 weeks.
