A Relative Bioavailability and Food Effect Study of TYRA-300-B01 Capsule and Tablet Formulations in Healthy Adult Participants

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About the study

The purpose of this study is to evaluate the relative bioavailability of capsule and tablet formulations of TYRA-300-B01, and to evaluate the safety, tolerability, and food effect of TYRA-300-B01 tablets in healthy adult participants.
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Who can take part

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

INCLUSION CRITERIA

Inclusion Criteria:

  1. * Males or females of non-childbearing potential, between 18 and 55 years of age
  2. * In good health, determined by no clinically significant findings from medical history, 12-lead electrocardiogram (ECG), vital signs, and clinical laboratory assessments
  3. * Body mass index (BMI) 18 to 32 kg/m\^2 (inclusive)
  4. * Cohorts 1 and 2 ethnicity requirements: none
  5. * Cohort 3 ethnicity requirements: first- or second-generation Japanese participants

EXCLUSION CRITERIA

Exclusion Criteria:

  1. * Significant history of any hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, immunologic, musculoskeletal disease, or allergic disease (as determined by the Investigator)
  2. * Any ocular condition likely to increase the risk of eye toxicity
  3. * Gastrointestinal disorders that will affect oral administration or absorption of TYRA-300-B01
  4. * Females of child-bearing potential and males who plan to father a child while enrolled in this study
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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
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Study Details


Contition
Healthy
Age (in years)
26 - 55
Phase
PHASE1
Participants Needed
60
Est. Completion Date
Jul 31, 2024
Treatment Type
INTERVENTIONAL

Sponsor
Tyra Biosciences, Inc
ClinicalTrials.gov NCT Identifier
NCT06006702
Study Number
TYR300-102

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