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Monoclonal Antibodies
LYS006 for Ulcerative Colitis
Phase 2
Waitlist Available
Research Sponsored by Novartis Pharmaceuticals
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up adverse events were reported from first dose of study treatment until end of study treatment plus 30 days post treatment, up to a maximum duration of approximately 86 days.
Awards & highlights
Study Summary
This trial is testing a new drug to treat ulcerative colitis. They want to see if it is safe and effective. If it is, they will continue developing it as a treatment.
Eligible Conditions
- Ulcerative Colitis
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ adverse events were reported from first dose of study treatment until end of study treatment plus 30 days post treatment, up to a maximum duration of approximately 86 days.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~adverse events were reported from first dose of study treatment until end of study treatment plus 30 days post treatment, up to a maximum duration of approximately 86 days.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Clinical Remission Rate at the End of the Study Treatment
Secondary outcome measures
Number of Participants With Treatment Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs)
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: LYS006Experimental Treatment1 Intervention
Experimental drug
Group II: PlaceboPlacebo Group1 Intervention
Placebo comparator
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Who is running the clinical trial?
Novartis PharmaceuticalsLead Sponsor
2,855 Previous Clinical Trials
4,197,720 Total Patients Enrolled
2 Trials studying Ulcerative Colitis
87 Patients Enrolled for Ulcerative Colitis
Frequently Asked Questions
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