A Study to Evaluate the Incidence of Hypersensitivity After Administration of Sugammadex in Healthy Participants (MK-8616-101)

A Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Evaluate the Incidence of Hypersensitivity After Repeated Single Dose Administration of Sugammadex (MK-8616) in Healthy Subjects

Patrocinadores

Patrocinador principal: Merck Sharp & Dohme Corp.

Fuente Merck Sharp & Dohme Corp.
Resumen breve

The purpose of this study is to assess the potential for hypersensitivity symptoms upon repeat exposure to sugammadex. Healthy participants will be randomized to one of three treatment arms: sugammadex 4 mg/kg, sugammadex 16 mg/kg or placebo. Participants will receive 3 single intravenous (IV) doses of their randomized treatment, with an approximately 5-week washout between Dose 1 and Dose 2 and between Dose 2 and Dose 3. Participants will be confined at the study center from the day before each dose until completion of the 24-hour post dose assessments.

Estado general Completed
Fecha de inicio January 3, 2014
Fecha de Terminación July 1, 2014
Fecha de finalización primaria July 1, 2014
Fase Phase 1
Tipo de estudio Interventional
Resultado primario
Medida Periodo de tiempo
Percentage of Participants With Adjudicated Symptoms of Hypersensitivity Up to approximately 28 days after last dose (approximately 14 weeks)
Resultado secundario
Medida Periodo de tiempo
Percentage of Participants With Adjudicated Anaphylaxis Up to approximately 28 days after last dose (approximately 14 weeks)
Inscripción 382
Condición
Intervención

Tipo de intervención: Drug

Nombre de intervención: Sugammadex

Descripción: Sugammadex 4 mg/kg or 16 mg/kg administered as a single IV bolus over 10 seconds

Tipo de intervención: Drug

Nombre de intervención: Placebo

Descripción: Placebo administered as a single IV bolus over 10 seconds

Etiqueta de grupo de brazo: Placebo

Elegibilidad

Criterios:

Inclusion Criteria:

- Male or non-pregnant and non-breast feeding female

- Females of childbearing potential must have a serum β-human chorionic gonadotropin (β-hCG) level consistent with non-pregnant state and agree to use (and/or have their partner use) two acceptable methods of birth control beginning at screening, throughout the trial (including washout intervals between treatment periods) and until after the post-study follow-up visit

- Females not of childbearing potential must be either a) postmenopausal (have not had a menstrual period for at least 1 year and have a follicle stimulating hormone [FSH] value in the postmenopausal range) or b) surgically sterile (i.e., have had hysterectomy, oophorectomy or tubal ligation)

- In good health based on medical history, laboratory tests and other assessments

- Body Mass Index (BMI) ≥19 and ≤32 kg/m^2

- Non-smoker or smokes ≤10 cigarettes/day or equivalent (2 pipes/day, 1 cigar/day) and agrees not to smoke while confined at the study center

Exclusion Criteria:

- Mentally or legally incapacitated, has significant emotional problems at the time of screening visit or expected during the conduct of the trial or has a history of clinically significant psychiatric disorder of the last 5 years

- History of clinically significant endocrine, gastrointestinal, cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary or major neurological abnormalities or diseases

- History of cancer (malignancy)

- History of significant multiple and/or severe allergies (e.g., food, drug, latex allergy), or has had an anaphylactic reaction or significant intolerability to prescription or non-prescription drugs or food

- Positive for hepatitis B surface antigen, hepatitis C antibodies or human immunodeficiency virus (HIV)

- Has had major surgery and/or donated or lost 1 unit of blood (approximately 500 mL) within 4 weeks prior to screening

- Has participated in another investigational trial within 4 weeks prior to screening

- Is unable to refrain from or anticipates the use of any medication, including prescription and non-prescription drugs or herbal remedies beginning approximately 2 weeks prior to administration of the initial dose of trial drug, throughout the trial (including washout intervals between treatment periods), until the post-study follow-up visit

- Has received subcutaneous or sublingual immunotherapy within the past 1 year

- Consumes >3 glasses of alcoholic beverages per day

- Consumes excessive amounts, defined as >6 servings of coffee, tea, cola, energy drinks, or other caffeinated beverages per day

- Currently a regular user (including "recreational use") of any illicit drugs or has a history of drug (including alcohol) abuse within approximately 12 months

- Has a recollection of previously receiving sugammadex, Bridion™, SCH 900616, ORG 25969, or MK-8616

- History of chronic urticaria or angioedema

- Is or has an immediate family member (spouse or children) who is a member of investigational site or sponsor staff directly involved with this trial

Género: All

Edad mínima: 18 Years

Edad máxima: 55 Years

Voluntarios Saludables: Accepts Healthy Volunteers

Oficial general
Apellido Papel Afiliación
Medical Director Study Director Merck Sharp & Dohme Corp.
Fecha de verificación

March 2019

Fiesta responsable

Tipo: Sponsor

Palabras clave
Tiene acceso ampliado No
Condición Examinar
Número de brazos 3
Grupo de brazo

Etiqueta: Sugammadex 4 mg/kg

Tipo: Experimental

Descripción: Administration of 3 single IV doses of sugammadex 4 mg/kg, with an approximately 5-week washout between Dose 1 and Dose 2 and between Dose 2 and Dose 3

Etiqueta: Sugammadex 16 mg/kg

Tipo: Experimental

Descripción: Administration of 3 single IV doses of sugammadex 16 mg/kg, with an approximately 5-week washout between Dose 1 and Dose 2 and between Dose 2 and Dose 3

Etiqueta: Placebo

Tipo: Placebo Comparator

Descripción: Administration of 3 single IV doses of placebo, with an approximately 5-week washout between Dose 1 and Dose 2 and between Dose 2 and Dose 3

Datos del paciente Yes
Información de diseño del estudio

Asignación: Randomized

Modelo de intervención: Parallel Assignment

Propósito primario: Treatment

Enmascaramiento: Triple (Participant, Investigator, Outcomes Assessor)

Fuente: ClinicalTrials.gov