Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

A Drug-Drug Interaction Study Between ATI-2173 and Tenofovir Disoproxil Fumarate in Healthy Subjects

3 de febrero de 2022 actualizado por: Antios Therapeutics, Inc

A Phase 1, Open-label, 2-cohort, Multiple Dose, Drug-drug Interaction, Safety and Tolerability, Fixed-sequence Study to Investigate the Potential Interaction Between ATI-2173 When Coadministered With Tenofovir Disoproxil Fumarate in Healthy Subjects

This study is a single-center, open-label, 2-cohort, multiple dose, fixed-sequence, DDI study in healthy adult subjects. Healthy volunteers will be administered multiple oral doses of ATI-2173 in combination with tenofovir disoproxil fumarate and assessed for safety and tolerability including blood tests to show how the body metabolizes and eliminates the investigational drug as well as how the investigational drug interacts with tenofovir disoproxil fumarate.

Descripción general del estudio

Estado

Terminado

Tipo de estudio

Intervencionista

Inscripción (Actual)

32

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Quebec
      • Montréal, Quebec, Canadá, H3P 3P1
        • Altasciences

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 59 años (Adulto)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  1. Provision of signed and dated Informed Consent Form (ICF)
  2. Stated willingness to comply with all study procedures (including ability and willingness to abstain from alcohol from 48 hours prior to the first study drug administration until discharge) and availability for the duration of the study
  3. Healthy adult male or female
  4. Aged between 18 and 59 years, inclusive
  5. Body mass index (BMI) within 18.5 kg/m2 to 30.0 kg/m2, inclusively
  6. Non- or ex-smoker (an ex-smoker is defined as someone who completely stopped using nicotine products for at least 180 days prior to the first study drug administration)
  7. Suitable veins for cannulation or repeated venipuncture as assessed by an Investigator at Screening Have no clinically significant diseases captured in the medical history or evidence of clinically significant findings on the physical examination (including vital signs) and/or ECG, as determined by an Investigator

9. Agrees to abstain from blood or plasma donation from the Screening visit until 3 months after the last study drug administration 10. If female, must meet one of the following criteria:

  1. Is of childbearing potential and agrees to use an acceptable contraceptive method. Acceptable contraceptive methods include:

    • Abstinence from heterosexual intercourse from Screening through to at least 60 days after the last dose of the study drug
    • Male partner vasectomized at least 180 days prior to Screening
    • Double-barrier method (eg, male condom, spermicide and diaphragm or cervical cap used simultaneously) from Screening through to at least 30 days after the last dose of the study drug
    • One of the following contraceptive methods with a barrier method (eg, male condom) from at least 28 days prior to the first study drug administration through to at least 60 days after the last dose of the study drug:
    • Systemic contraceptives (combined birth control pills, injectable/implant/insertable hormonal birth control products, transdermal patch)
    • Intrauterine device (with or without hormones) If systemic contraceptives are used, must agree to use an additional acceptable non-hormonal method during the study and for at least 60 days after the last dose of the study drug Or
  2. Is of non-childbearing potential, defined as surgically sterile (ie, has undergone complete hysterectomy, bilateral oophorectomy, or tubal ligation/occlusion) or in a postmenopausal state (at least 1 year without menses without an alternative medical condition prior to Screening), as confirmed by follicle-stimulating hormone levels (≥ 40 mIU/mL).

    11. A male study subject that engages in sexual activity that has the risk of pregnancy must:

    • Agree to use a double-barrier method (eg, male condom, spermicide and diaphragm or cervical cap used simultaneously) or be abstinent from heterosexual intercourse from Screening to at least 90 days after the last study drug administration or be unable to procreate; defined as surgically sterile (i.e. has undergone a vasectomy at least 180 days prior to Screening) AND
    • Agree to not donate sperm during the study and for at least 90 days after the last study drug administration 12. Body weight ≥35 kg (≥77 lb)

    Exclusion Criteria:

    1. Female who is lactating
    2. Female who is pregnant according to the pregnancy test at Screening or prior to the first study drug administration
    3. Pulse rate less than 50 beats per minute or more than 100 beats per minute at Screening or prior to the first study drug administration unless deemed not clinically significant by the Investigator
    4. Blood pressure below 100/60 mmHg or higher than 140/90 mmHg at Screening or prior to the first study drug administration unless deemed not clinically significant by the Investigator
    5. History of hypersensitivity to ATI-2173, clevudine, tenofovir, or any related products (including excipients of the formulations) as well as severe hypersensitivity reactions (like angioedema) to any drugs
    6. Presence or history of significant gastrointestinal, liver or kidney disease, or surgery that may affect drug bioavailability including but not limited to cholecystectomy
    7. History of significant cardiovascular, pulmonary, hematologic, neurological, psychiatric, endocrine, immunologic or dermatologic disease, in the opinion of an Investigator
    8. Presence of clinically significant ECG abnormalities at Screening or prior to study drug administration, in the opinion of an Investigator
    9. Presence of clinically significant muscle disorders, myopathies or other forms of liver disease, in the opinion of an Investigator
    10. Estimated glomerular filtration rate (eGFR) < 80 mL/min/1.73 m2 using the Modification of Diet in Renal Disease (MDRD) equation at Screening or < 60 mL/min/1.73 m2 on Day -1
    11. Hemoglobin value below the lower limit of the reference laboratory at Screening or prior to study drug administration
    12. Unexplained persistent elevations of serum transaminases or creatine kinase (CK) levels at Screening or prior to study drug administration
    13. Maintenance therapy with any drug or significant history of drug dependency or alcohol abuse (> 3 units of alcohol per day, intake of excessive alcohol, acute or chronic)
    14. Any clinically significant illness in the 28 days prior to the first study drug administration
    15. Use of any prescription drugs (except systemic contraception and intrauterine devices) in the 30 days prior to the first study drug administration, that in the opinion of an Investigator would put into question the status of the participant as healthy
    16. Use of St. John's wort in the 30 days prior to the first study drug administration
    17. Use of quinine-containing products (eg, tonic water), grapefruit products, pomelo products, Seville orange products, including supplements containing Citrus aurantium or "bitter orange", in the 14 days prior to the first study drug administration
    18. Any history of latent or active tuberculosis
    19. Positive screening tuberculosis blood test
    20. Immunization with a COVID-19 vaccine in the 14 days prior to the first study drug administration
    21. Scheduled immunization with a COVID-19 vaccine (first or second dose) during the study that, in the opinion of an investigator, could potentially interfere with subject participation, subject safety, study results, or any other reason
    22. Positive test result for alcohol and/or drugs of abuse at Screening or prior to the first drug administration
    23. Positive test results for HIV-1/HIV-2 antibodies, hepatitis B surface antigen or hepatitis C antibody at Screening
    24. Any other clinically significant abnormalities in laboratory test results at Screening or prior to the first drug administration that would, in the opinion of an Investigator, increase the subject's risk of participation, jeopardize complete participation in the study, or compromise interpretation of study data.
    25. Inclusion in a previous group for this clinical study
    26. Participation in another clinical study with a non-biologic Investigational Product (IP) or new formulation of a marketed non-biologic drug in the 30 days prior to the first study drug administration
    27. Participation in another clinical study with a biologic (marketed or investigational) in the 90 days or 5 half-lives (whichever is longer) prior to the first study drug administration
    28. Donation of 50 mL or more of blood in the 28 days prior to the first study drug administration
    29. Donation of 500 mL or more of blood (Canadian Blood Services, Hema-Quebec, clinical studies, etc.) in the 56 days prior to the first study drug administration
    30. History of pathologic fracture or other risk factors for osteoporosis or bone loss

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: No aleatorizado
  • Modelo Intervencionista: Asignación Secuencial
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: ATI-2173.
ATI-2173
ATI-2173 is a liver-targeted phosphoramidate oral prodrug of clevudine designed to enhance anti-HBV activity while decreasing systemic exposure to clevudine. It will be dosed as a capsule by mouth
Experimental: Tenofovir Disoproxil Fumarate
Tenofovir disoproxil fumarate
Tenofovir is an oral nucleotide analogue reverse transcriptase inhibitor used for chronic hepatitis B virus. It will be dosed as a tablet by mouth
Otros nombres:
  • Viread 300 mg

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Cmax of ATI-2173, clevudine, and M1 in plasma
Periodo de tiempo: Through end of study, approximately 3 months
Through end of study, approximately 3 months
AUCtau of ATI-2173, clevudine, and M1 in plasma
Periodo de tiempo: Through end of study, approximately 3 months
Through end of study, approximately 3 months
AUC0-t of ATI-2173, clevudine, and M1 in plasma
Periodo de tiempo: Through end of study, approximately 3 months
Through end of study, approximately 3 months
Cmax of tenofovir
Periodo de tiempo: Through end of study, approximately 3 months
Through end of study, approximately 3 months
Cmin,ss of tenofovir
Periodo de tiempo: Through end of study, approximately 3 months
Through end of study, approximately 3 months
AUC0-tau of tenofovir
Periodo de tiempo: Through end of study, approximately 3 months
Through end of study, approximately 3 months
AUC0-t of tenofovir
Periodo de tiempo: Through end of study, approximately 3 months
Through end of study, approximately 3 months

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Number of Adverse Events
Periodo de tiempo: Through end of study, approximately 3 months
Through end of study, approximately 3 months

Otras medidas de resultado

Medida de resultado
Periodo de tiempo
Plasma trough concentrations of tenofovir, ATI-2173, clevudine, and M1
Periodo de tiempo: Days 18, 19, 20 and 21
Days 18, 19, 20 and 21

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

27 de octubre de 2021

Finalización primaria (Actual)

23 de diciembre de 2021

Finalización del estudio (Actual)

23 de diciembre de 2021

Fechas de registro del estudio

Enviado por primera vez

27 de octubre de 2021

Primero enviado que cumplió con los criterios de control de calidad

16 de noviembre de 2021

Publicado por primera vez (Actual)

30 de noviembre de 2021

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

4 de febrero de 2022

Última actualización enviada que cumplió con los criterios de control de calidad

3 de febrero de 2022

Última verificación

1 de febrero de 2022

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Suscribir