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First-In-Human Study of BBT-401-1S Following Single and Multiple Ascending Doses in Healthy Volunteers

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ClinicalTrials.gov Identifier: NCT03482648
Recruitment Status : Completed
First Posted : March 29, 2018
Last Update Posted : December 28, 2018
Sponsor:
Collaborator:
KCRN Research, LLC
Information provided by (Responsible Party):
Bridge Biotherapeutics, Inc.

Brief Summary:
This clinical trial is the first-in-human study of BBT-401-1S. The purpose of this phase 1 study is to assess the safety and tolerability of single and multiple ascending oral doses of BBT-401-1S in healthy adult subjects.

Condition or disease Intervention/treatment Phase
Ulcerative Colitis Drug: BBT-401-1S, Single dose Drug: BBT-401-1S, Multiple doses Drug: Placebo Phase 1

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 80 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Phase I, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety, Tolerability and Pharmacokinetics of Novel Oral Peptide BBT-401-1S Following Single and Multiple Ascending Doses in Healthy Adult Subjects
Actual Study Start Date : March 20, 2018
Actual Primary Completion Date : September 26, 2018
Actual Study Completion Date : October 3, 2018

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Single Ascending Doses Drug: BBT-401-1S, Single dose
Single dose of BBT-401-1S, 7 dose levels, oral capsule

Drug: Placebo
Placebo matched to BBT-401-1S, oral capsule

Experimental: Multiple Ascending Doses Drug: BBT-401-1S, Multiple doses
Multiple doses of BBT-401-1S, 7 days, 3 dose levels, oral capsule

Drug: Placebo
Placebo matched to BBT-401-1S, oral capsule




Primary Outcome Measures :
  1. The number and severity of treatment emergent adverse events (TEAEs) [ Time Frame: 7 days after the last dose ]
    To assess the safety and tolerability of single and multiple ascending oral doses of BBT-401-1S in healthy adult subjects.


Secondary Outcome Measures :
  1. Maximum plasma concentration (Cmax) [ Time Frame: 72 hours after the last dose ]
    To assess Cmax of single and multiple ascending oral doses of BBT-401-1S in healthy adult subjects.

  2. Area under the curve (AUC) [ Time Frame: 72 hours after the last dose ]
    To assess AUC of single and multiple ascending oral doses of BBT-401-1S in healthy adult subjects.

  3. Maximum plasma concentration (Cmax) under fed conditions [ Time Frame: 72 hours after the last dose ]
    To assess Cmax of single oral dose under fed conditions

  4. Area under the curve (AUC) under fed conditions [ Time Frame: 72 hours after the last dose ]
    To assess AUC of single oral dose under fed conditions



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Ages Eligible for Study:   19 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Healthy adult male and/or female (non-childbearing potential only), 19 to 55 years of age, inclusive, at screening.
  2. Continuous non-smoker who has not used nicotine-containing products for at least 3 months prior to the first dose and throughout the study.
  3. Body mass index (BMI) ≥ 18.5 and ≤ 32.0 (kg/m2) at screening and weight ≥ 50 kg at screening.
  4. Medically healthy with no clinically significant medical history, physical examination, laboratory profiles, vital signs or ECGs, as deemed by the PI.
  5. No clinically significant history or presence of ECG findings as judged by the PI or qualified designee at screening and check-in.
  6. For a female, must be of non-childbearing potential and therefore must have undergone one of the following sterilization procedures, at least 6 months prior to the first dose:

    1. hysteroscopic sterilization;
    2. bilateral tubal ligation or bilateral salpingectomy;
    3. hysterectomy;
    4. bilateral oophorectomy; or be postmenopausal with amenorrhea for at least 1 year prior to the first dose and follicle-stimulating hormone (FSH) serum levels consistent with postmenopausal status as per PI judgment.
  7. A non-vasectomized, male subject must agree to use a condom with spermicide or abstain from sexual intercourse during the study until 90 days beyond the last dose of study drug. (No restrictions are required for a vasectomized male provided his vasectomy has been performed 4 months or more prior to the first dose of study drug. A male who has been vasectomized less than 4 months prior to the first dose must follow the same restrictions as a non-vasectomized male).
  8. If male, must agree to not donate sperm from the first dose until 90 days after dosing.
  9. Must have the ability to understand and sign a written informed consent form, which must be obtained prior to initiation of study procedures.

Exclusion Criteria:

  1. Subject is mentally or legally incapacitated or has significant emotional problems at the time of the screening visit or expected during the conduct of the study.
  2. History or presence of clinically significant medical or psychiatric condition or disease in the opinion of the PI.
  3. History of any illness that, in the opinion of the PI, might confound the results of the study or poses an additional risk to the subject by their participation in the study.
  4. History or presence of alcoholism or drug abuse within the past 2 years prior to the first dose or regular alcohol consumption within 6 months prior to the first dose with an average weekly intake of greater than 21 glasses/units per week for males or 14 glasses/units per week for females, with one unit = 150 mL of wine or 360 mL of beer or 45 mL of 45% alcohol.
  5. History or presence of hypersensitivity or idiosyncratic reaction to the study drug(s) or related compounds.
  6. History of sensitivity to heparin or heparin-induced thrombocytopenia.
  7. Active or latent tuberculosis.
  8. Estimated creatinine clearance <80 mL/min at screening.
  9. Liver function tests (serum ALT, AST, alkaline phosphatase) and serum bilirubin (total and direct) > ULN.
  10. Absolute neutrophil count < 1500 cells/mm3.
  11. White blood cell count < 3500 cells/mm3.
  12. Haemoglobin levels < 0.5 mg/dL below the lower limit of normal.
  13. Seated heart rate is lower than 40 bpm or higher than 99 bpm at screening.
  14. Female subjects of childbearing potential.
  15. Female subjects who are pregnant or lactating.
  16. Positive urine drug or alcohol results at screening or check-in.
  17. Positive urine cotinine at screening.
  18. Positive results at screening for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C antibodies (HCV).
  19. Unable to refrain from or anticipates the use of any drug, including prescription and non-prescription medications, herbal remedies, or vitamin supplements beginning approximately 14 days prior to the first dose and throughout the study.. Hormone replacement therapy will not be allowed. After first dosing, acetaminophen (up to 2 g per 24 hours) may be administered at the discretion of the PI or designee.
  20. Has been on a diet incompatible with the on-study diet, in the opinion of the PI, within the 28 days prior to the first dose and throughout the study.
  21. Donation of blood or significant blood loss within 56 days prior to the first dose.
  22. Plasma donation within 7 days prior to the first dose.
  23. Exposure to more than four new chemical entities within 12 months prior to first dosing day.
  24. The subject has participated in a clinical trial and has received an investigational product within 30 days, or 5 half-lives of the investigational product (whichever is longer) of the first dose of study drug in the current study.
  25. Any condition or circumstance, in the opinion of the PI, which may make the subject unlikely to complete the study or comply with study procedures and requirements, or may pose a risk to the subject's safety.
  26. Subject has recent history (within 2 weeks of Day -1) of less than 1 bowel movement every 2 days.
  27. Subject has recent history (within 2 weeks of Day -1) of abnormal bowel movements, such as diarrhea, loose stools, or constipation.

    Stage 1 Only:

  28. Is lactose intolerant.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03482648


Locations
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United States, Nebraska
Celerion
Lincoln, Nebraska, United States, 68502
Sponsors and Collaborators
Bridge Biotherapeutics, Inc.
KCRN Research, LLC
Investigators
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Study Director: GwangHee Lee, Ph.D. Bridge Biotherapeutics, Inc.

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Responsible Party: Bridge Biotherapeutics, Inc.
ClinicalTrials.gov Identifier: NCT03482648     History of Changes
Other Study ID Numbers: BBT401-UC-US01
First Posted: March 29, 2018    Key Record Dates
Last Update Posted: December 28, 2018
Last Verified: December 2018

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Bridge Biotherapeutics, Inc.:
Pellino-1

Additional relevant MeSH terms:
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Colitis, Ulcerative
Colitis
Gastroenteritis
Gastrointestinal Diseases
Digestive System Diseases
Inflammatory Bowel Diseases
Colonic Diseases
Intestinal Diseases