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 Trial to Assess TEV-56286 at Different Doses in Healthy Participants

3 de septiembre de 2026 actualizado por: Teva Branded Pharmaceutical Products R&D LLC

A Phase 1 Double-Blind, Randomized, Placebo-Controlled, Single and Multiple Escalating Dose Trial in Healthy Participants to Assess Pharmacokinetics, Safety, and Tolerability of TEV-56286 at Clinical and Supratherapeutic Doses

The purpose of the trial is to evaluate the pharmacokinetics, safety, and tolerability of TEV-56286 at different doses.

The main objective is to describe how TEV-56286 is absorbed, distributed, and removed from the body (the pharmacokinetics) following administration of TEV-56286 in single doses of increasing amounts and multiple doses in healthy participants.

A secondary objective is to assess the safety of TEV-56286 and how well it is tolerated.

The estimated duration for participants in Part 1 with Single Ascending Dose is approximately 58 days; including up to 45 days of screening, a 4-day in-clinic period, and follow-up 8+/-1 days post discharge from the clinical unit.

The estimated duration for participants in Part 2 with Multiple Ascending Dose is approximately 64 days; including up to 45 days of screening, a 10-day in-clinic period, and follow-up 8+/-1 days post discharge from the clinical unit.

Descripción general del estudio

Estado

Reclutamiento

Condiciones

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

69

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.

Estudio Contacto

  • Nombre: Teva U.S. Medical Information
  • Número de teléfono: 1-888-483-8279
  • Correo electrónico: USMedInfo@tevapharm.com

Ubicaciones de estudio

    • Florida
      • Miramar, Florida, Estados Unidos, 33025
        • Reclutamiento
        • Teva Investigational Site 12174

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

  • Adulto

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • Participant is a healthy male or female with a body weight of ≥50 kg for males and ≥45 kg for females, and body mass index (BMI) of 18.5 to 32.0 kg/m2 inclusive.
  • Participant is 18 to 60 years of age inclusive, at the time of signing the informed consent form (ICF).
  • Female participants are eligible to participate if she is not pregnant or breastfeeding, and 1 of the following conditions applies:
  • A woman of non-child bearing potential (WONCBP) as defined: Female participants who are either surgically (documented hysterectomy, bilateral oophorectomy, or bilateral salpingectomy) or congenitally sterile, or at least 1 year postmenopausal (no menses for at least 12 months without an alternative medical cause plus an increased concentration of follicle stimulating hormone [FSH] within the menopausal range in women not using hormonal contraception or hormonal replacement therapy).
  • A woman of childbearing potential (WOCBP) and using a contraceptive method that is highly effective (with a failure rate of <1% per year), used consistently and correctly. The acceptable contraceptive regimens in this trial are: non-hormonal intrauterine device (IUD) used for at least 2 consecutive months prior to dosing and willing to continue until at least 28 days after last dose of investigational medicinal product (IMP), bilateral tubal occlusion, and/or azoospermic partner (vasectomized or due to a medical cause). A WOCBP must have a negative highly sensitive serum pregnancy test within 24 hours before the first dose of IMP. The participant must be excluded from participation if the serum pregnancy result is positive.
  • Male participants are eligible to participate if they are azoospermic (vasectomized or due to a medical cause) or, alternatively, agree to the following during the trial period, from admission (day -1) and for at least 28 days after last dose of IMP.

Refrain from donating sperm, in addition to following:

  • EITHER be abstinent from heterosexual intercourse as their preferred and usual lifestyle (abstinent on a long term and persistent basis) and agree to remain abstinent.
  • OR must agree to use contraception/barrier as detailed below:

    • Agree to use a male condom with female partner using an additional highly effective contraceptive method with a failure rate of <1% per year when having sexual intercourse with a WOCBP who is not currently pregnant.
    • Agree to use a male condom when having sexual intercourse with a pregnant partner.

NOTE-Additional criteria apply, please contact the investigator for more information

Exclusion Criteria:

  • Participant presents with or has a history of clinically significant diseases of the renal, hepatic, gastrointestinal, cardiovascular, musculoskeletal system, or presence/history of clinically significant immunological, endocrine, metabolic diseases, neurological, psychiatric, or immunological disorder(s), or a history of any illness that, in the opinion of the Principal Investigator, might pose additional risk to the participant by participation in the trial or confound the results of the trial.
  • Participant presents with a major trauma or surgery during the 60 days prior to screening or at any time between screening and the first dose of IMP, or surgery scheduled during the trial including follow-up period.
  • The participant has a history of any malignant disease (except for treated and cured skin basal cell carcinoma at least 12 months prior to screening).
  • Participant has a known drug hypersensitivity reaction to the active component of IMP, or one of its excipients, or any compound listed as being present in a trial formulation.
  • Participant has a personal or family history of arrhythmia, long QT syndrome, or sudden unexplained death in a first-degree relative before the age of 40; or personal history of syncope, myocardial infarction, cerebrovascular accident, or previous treatment for high blood pressure (BP).
  • Participant has an alkaline phosphatase (ALP), alanine aminotransferase (ALT), gamma-glutamyl transferase (GGT), aspartate aminotransferase (AST), or total bilirubin above the upper limit of normal (ULN).
  • Participant has a history of alcohol, drug, or any other substance dependence (with the exception of nicotine or caffeine) as defined by the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (American Psychiatric Association 2013) or are unwilling to comply with the restricted food or beverages during the trial.
  • Participant is a current smoker, has smoked in the last 6 months, is planning to start smoking during the trial, uses tobacco, or uses other nicotine-containing products (eg, snuff, nicotine patch, nicotine chewing gum, mock cigarettes, e-cigarettes, vaping devices, inhalers), or has a positive urine cotinine test.

NOTE-Additional criteria apply, please contact the investigator for more information

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: Otro
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación Secuencial
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Group 1: Single Ascending Dose (SAD1)
placebo coincidente
oral administration
Otros nombres:
  • emrusolmin, anle138b
Experimental: Group 2: Single Ascending Dose (SAD2)
placebo coincidente
oral administration
Otros nombres:
  • emrusolmin, anle138b
Experimental: Group 3: Single Ascending Dose (SAD3)
placebo coincidente
oral administration
Otros nombres:
  • emrusolmin, anle138b
Experimental: Group 4: Single Ascending Dose (SAD4)
placebo coincidente
oral administration
Otros nombres:
  • emrusolmin, anle138b
Experimental: Group 5: Multiple Ascending Dose (MAD1)
oral administration
Otros nombres:
  • emrusolmin, anle138b
Experimental: Group 6: Multiple Ascending Dose (MAD2)
placebo coincidente
oral administration
Otros nombres:
  • emrusolmin, anle138b

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
SAD: Time to maximum observed plasma drug concentration (tmax) of TEV-56286
Periodo de tiempo: Day 1 to Day 3
Day 1 to Day 3
SAD: Maximum observed plasma concentration (Cmax) of TEV-56286
Periodo de tiempo: Day 1 to Day 3
Day 1 to Day 3
SAD: Area Under the Plasma Drug Concentration-Time Curve from Time 0 to the Time of the Last Measurable Concentration (AUC0-t) of TEV-56286
Periodo de tiempo: Day 1 to Day 3
Day 1 to Day 3
SAD: Area Under the Plasma Drug Concentration-Time Curve from Time 0 to Infinity (AUC0-inf) of TEV-56286
Periodo de tiempo: Day 1 to Day 3
Day 1 to Day 3
MAD: tmax of TEV-56286
Periodo de tiempo: Day 7 to Day 9
Day 7 to Day 9
MAD: Cmax of TEV-56286
Periodo de tiempo: Day 7 to Day 9
Day 7 to Day 9
MAD: AUC0-t of TEV-56286
Periodo de tiempo: Day 7 to Day 9
Day 7 to Day 9
MAD: Area Under the Plasma Drug Concentration-Time Curve for the Defined Interval Between Doses (AUC0-tau) of TEV-56286
Periodo de tiempo: Day 7 to Day 8
Day 7 to Day 8

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Number of participants with at least 1 treatment-emergent adverse event
Periodo de tiempo: Up to Day 17
Up to Day 17
Number of participants who did not complete the trial due to an adverse event
Periodo de tiempo: Up to Day 17
Up to Day 17

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Director de estudio: Teva Medical Expert, MD, Teva Branded Pharmaceutical Products R&D LLC

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)

26 de junio de 2026

Finalización primaria (Estimado)

15 de enero de 2027

Finalización del estudio (Estimado)

22 de enero de 2027

Fechas de registro del estudio

Enviado por primera vez

23 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

23 de junio de 2026

Publicado por primera vez (Actual)

30 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

8 de septiembre de 2026

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

3 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • TV56286-PK-10202

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Qualified researchers may request access to patient level data and related study documents including the study protocol and the statistical analysis plan. Requests will be assessed for scientific merit, product approval status, and conflicts of interest. If the request is approved, patient level data will be de-identified and study documents will be redacted to protect the privacy of trial participants and to protect commercially confidential information. Please email USMedInfo@tevapharm.com to make your request.

Información sobre medicamentos y dispositivos, documentos del estudio

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

Sí

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. .