Study of TAVO101 in Healthy Volunteers

Sponsor
Tavotek Biotherapeutics (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05298046
Collaborator
(none)
42
1
4
12.5
3.4

Study Details

Study Description

Brief Summary

This is a Phase 1, single ascending dose study designed to investigate TAVO101, administered as an IV infusion in healthy subjects. This study is designed to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of TAVO101.

Condition or Disease Intervention/Treatment Phase
  • Drug: Experimental: TAVO101
  • Other: Other: Placebo
Phase 1

Detailed Description

This is a Phase 1, randomized, double-blind, placebo-controlled, single ascending dose (SAD), single site study. Six subjects will be enrolled into each of the 7 dosing cohorts. Subjects will be randomized at a ratio of 2:1 to receive TAVO101 or placebo. Two sentinel subjects will be utilized (1 active:1 placebo) in each cohort in a manner designed to maintain the blind. Subjects will be evaluated for safety throughout the study up through day 196.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
42 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Prevention
Official Title:
A Phase 1, Randomized, Placebo-Controlled, Double-Blind, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of TAVO101 in Adult Healthy Subjects
Anticipated Study Start Date :
Apr 15, 2022
Anticipated Primary Completion Date :
Nov 15, 2022
Anticipated Study Completion Date :
May 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: TAVO101: Low dose

TAVO101: TAVO101 single ascending dose IV infusion.

Drug: Experimental: TAVO101
TAVO101 single ascending dose IV infusion.
Other Names:
  • TAVO101
  • Experimental: TAVO101: Medium dose

    TAVO101: TAVO101 single ascending dose IV infusion.

    Drug: Experimental: TAVO101
    TAVO101 single ascending dose IV infusion.
    Other Names:
  • TAVO101
  • Experimental: TAVO101: High dose

    TAVO101: TAVO101 single ascending dose IV infusion.

    Drug: Experimental: TAVO101
    TAVO101 single ascending dose IV infusion.
    Other Names:
  • TAVO101
  • Placebo Comparator: Placebo

    Placebo single ascending dose IV infusion.

    Other: Other: Placebo
    Placebo single ascending dose IV infusion.

    Outcome Measures

    Primary Outcome Measures

    1. The severity of adverse effects according to the National Cancer Institute's Common Terminology Criteria for AEs, Version 5.0 [Time Frame: Day 1 through Day 196] [196 days]

      To investigate the safety and tolerability of TAVO101 in healthy volunteers.

    2. Changes in vital signs including oral temperature or tympanic temperature (C°) [Time Frame: Day 1 through Day 196] [196 days]

      To investigate the safety and tolerability of TAVO101 in healthy volunteers.

    3. Changes in vital signs including respiratory rate (breaths per minute) [Time Frame: Day 1 through Day 196] [196 days]

      To investigate the safety and tolerability of TAVO101 in healthy volunteers.

    4. Changes in vital signs including systolic and diastolic blood pressure (mmHg) [Time Frame: Day 1 through Day 196] [196 days]

      To investigate the safety and tolerability of TAVO101 in healthy volunteers.

    5. Changes in vital signs including pulse rate (beats per minute) [Time Frame: Day 1 through Day 196] [196 days]

      To investigate the safety and tolerability of TAVO101 in healthy volunteers.

    Secondary Outcome Measures

    1. Immunogenicity of TAVO101 [ Time Frame: Day 1 through Day 196 ] [196 days]

      Incidence of anti-drug antibodies (ADA) following dosing of TAVO101

    2. Cmax (Maximum observed serum concentration ) [ Time Frame: Day 1 through Day 196 ] [196 days]

      To investigate the pharmacokinetics of TAVO101 in healthy volunteers.

    3. tmax (time that Cmax was observed) [ Time Frame: Day 1 through Day 196 ] [196 days]

      To investigate the pharmacokinetics of TAVO101 in healthy volunteers.

    4. AUC-last (Area under the serum concentration-time curve from time 0 to the time of the last quantifiable concentration; calculated using the linear/log trapezoid rule) [ Time Frame: Day 1 through Day 196 ] [196 days]

      To investigate the pharmacokinetics of TAVO101 in healthy volunteers.

    5. AUC-inf (Area under the serum concentration-time curve from time 0 extrapolated to infinity) [ Time Frame: Day 1 through Day 196 ] [196 days]

      To investigate the pharmacokinetics of TAVO101 in healthy volunteers.

    6. AUC0-t (Area under the serum concentration-time curve from time 0 to time t) [ Time Frame: Day 1 through Day 196 ] [196 days]

      To investigate the pharmacokinetics of TAVO101 in healthy volunteers.

    7. t½ (Terminal elimination half-life) [ Time Frame: Day 1 through Day 196 ] [196 days]

      To investigate the pharmacokinetics of TAVO101 in healthy volunteers.

    8. λz (Terminal elimination rate constant) [ Time Frame: Day 1 through Day 196 ] [196 days]

      To investigate the pharmacokinetics of TAVO101 in healthy volunteers.

    9. CL (Systemic clearance) [ Time Frame: Day 1 through Day 196 ] [196 days]

      To investigate the pharmacokinetics of TAVO101 in healthy volunteers.

    10. Vd (Volume of distribution) [ Time Frame: Day 1 through Day 196 ] [196 days]

      To investigate the pharmacokinetics of TAVO101 in healthy volunteers.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Males and females ≥ 18 and ≤ 65 years of age, inclusive.

    • Subjects must have a body weight range of ≥50 kg and≤100 kg, inclusive, and BMI ≥ 18.0 and ≤ 30.0 kg/m2, inclusive at Screening and Day-1.

    • Subjects must be healthy based on clinical laboratory tests performed at Screening and Day-1.

    • Females of childbearing potential who are sexually active with a male partner must agree to use a highly effective method of contraception from Screening through 196 days after the final dose of study drug.

    • Males who are sexually active and whose partners are females of childbearing potential must agree to use condoms from Screening through 196 days, after administration of the last dose of study drug and their partners must be willing to use a highly effective method of contraception from Screening through 196 days after the last dose of study drug.

    • Males must agree to not donate sperm from Screening through 196 days, after the last dose of study drug administration.

    • Subjects may be social smokers, defined as <5 cigarettes/month in last 6 months and must have negative cotinine test at Screening and check-in.

    • Subjects will be considered eligible according to the following tuberculosis screening criteria's.

    • Subjects must sign an Informed Consent Form.

    Exclusion Criteria:
    • Positive pregnancy test at Screening or baseline or is lactating.

    • History or presence of conditions which, in the judgment of the investigator, are known to interfere with the absorption, distribution, metabolism, or excretion of drugs.

    • History or presence of conditions that may place the subject at increased risk as determined by the investigator.

    • Subject has clinically significant laboratory abnormalities, or other clinically significant findings in the opinion of the investigator.

    • Subject currently has or has had a history of any clinically significant medical illness or medical disorders the investigator considers should exclude the subject.

    • Subject has a QT corrected according to Fridericia's formula (QTcF) interval >450 msec (for males) or >470 msec (for females), has a complete left or right bundle branch block, or has a history or current evidence of additional risk factors for Torsades de Pointes.

    • History of surgery or major trauma within 16 weeks of Screening, or will not have fully recovered from surgery, or has surgery planned during the time the subject is expected to participate in the study, or within 17 weeks after the last dose of study drug administration.

    • Subject plans to undergo non-major elective surgery within 5 weeks prior to study drug administration through EOS.

    • Subject has a known or suspected intolerance or hypersensitivity to any components of the formulation of TAVO101 and its excipients used in this study.

    • Subject has known hypersensitivity or severe allergies to food and or medication of clinical significance in the opinion of the investigator.

    • History of alcohol abuse (i.e., more than 3 drinks per day), illicit drug use, physical dependence to any opioid, or any history of drug abuse or addiction within 12 months of Screening.

    • Use of prescription medications (including hormone replacement therapy) within 14 days prior to administration of the study drug. By exception, prescription drugs, such as hormonal birth control, will be permitted.

    • Use of over-the-counter drugs (including herbal preparations) within 7 days or 5 half-lives (if known), whichever is longer, prior to administration of the study drug.

    • Has received a vaccination within 14 days prior to administration of the study drug.

    • Has taken other investigational drugs or participated in any clinical study within 30 days or 5 half-lives (if known) of the investigational drug's PK, PD, or biological activity.

    • Significant blood loss (>450mL) or has donated 1 or more units of blood or plasma within 6 weeks prior to study participation.

    • Strenuous activity within 48 hours prior to CRU admission.

    • Consumption of alcohol or caffeine-containing food or beverages within 48 hours prior to CRU admission.

    • Positive urine drugs of abuse, alcohol, or cotinine screen.

    • Positive test for HIV-1 or HIV-2 antibodies.

    • Positive test for hepatitis B virus or hepatitis C virus consistent with current infection.

    • Subject has liver function tests> 1.5x upper limit of normal (i.e., AST, ALT).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 CMAX Clinical Research Pty Ltd Adelaide South Australia Australia 5000

    Sponsors and Collaborators

    • Tavotek Biotherapeutics

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Tavotek Biotherapeutics
    ClinicalTrials.gov Identifier:
    NCT05298046
    Other Study ID Numbers:
    • 59870001
    First Posted:
    Mar 28, 2022
    Last Update Posted:
    Mar 28, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Mar 28, 2022