A Study to Evaluate the Efficacy, Safety and Pharmacokinetics of CDI-988 in Healthy Adults After Challenge With Snow Mountain Virus
Recruiting
Phase 1
Phase 2
Interventional Study
Norovirus
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 49
- Sex
- Any
- Trial phase
- Phase 1/2
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 40 (estimated)
- Sponsor
- Cocrystal Pharma, Inc. · Industry
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About This Trial
Participants in this study will be given either CDI-988 or placebo orally before receiving a norovirus challenge virus and continuing for 5 days. Participants will not know whether they are getting placebo or CDI-988. The study will evaluate how well CDI-988 compared to placebo can reduce the incidence of clinical symptoms after a challenge with norovirus. The amount of virus in stool samples will…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Healthy male or non-pregnant female
* Aged 18 to 49 years
* Good state of health
* Known fucosyl transferase 2 (FUT2) secretor status
Exclusion Criteria:
* History of participation in any norovirus challenge or vaccine clinical trial
* Receipt or planned receipt of any non-l…
Contacts