- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01874314
Effects of SQ109 on QTc Interval in Healthy Subjects
Phase 1 Crossover Study to Assess the Effects of SQ109 on QTc Interval in Healthy Subjects
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Fase
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
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Ohio
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Cleveland, Ohio, Estados Unidos, 44106-1716
- Case Western Reserve University - Case Medical Center - Infectious Disease & HIV Medicine
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Men and women aged 18 to 45 years, inclusive.
- Ability to understand the consent process and procedures.
- Informed consent obtained and signed.
- Comprehension of the study objectives and procedures which will be determined by the recruiter using a series of questions after explaining the procedures.
- Subject agrees to be available for all study visits and is able to comply with protocol requirements for the entire duration of the study.
- Subject agrees not to participate in another clinical trial at any time during the study period.
- Subjects who have a body mass index (BMI) >/=18 kg/m^2 and </= 35 kg/m^2
- General good health, without current medical illness or clinically significant abnormal physical examination findings that classify the subject as other than healthy as determined by study investigators
- Negative serum pregnancy test at screening and a negative urine pregnancy test on the day of admittance to the inpatient phase for all female subjects of child bearing potential.
- Negative urine toxicity screen for alcohol, marijuana, cocaine metabolite, amphetamines, opiates, PCP, barbiturates, and benzodiazepines.
- Agreement by subjects with reproductive potential to use an adequate method of contraception during the study and for 90 days after study drug administration. Female subjects must agree to the use of two reliable methods of contraception while receiving study drug and for 90 days after study drug administration, which can include: condoms, spermicidal gel, diaphragm, hormonal or non-hormonal intrauterine device, surgical sterilization, oral contraceptive pill, and depot progesterone injections. If a male subject is heterosexually active, the subject and his partner must use at least two forms of the listed contraceptive methods.
Exclusion Criteria:
Subjects meeting any exclusion criteria at baseline will be excluded from study partcipation.
Note that individuals with a history of cardiac arrhythmias will not be included as subjects in this study.
Medical condition that precludes participation, including the following:
- Hypertension with confirmed systolic blood pressure >140 mmHg or confirmed diastolic blood pressure >90 mmHg, measured after 10 - 15 minutes of rest.
- Morbid obesity (BMI>35)
- Current diagnosis of pulmonary disease including latent TB
- Current diagnosis of asthma, which has required use of asthma medications within the past year
- History of or current diagnosis of diabetes
- Autoimmune disorder, such as lupus, Wegener's, rheumatoid arthritis
- History of malignancy except low-grade skin cancer, (i.e., basal cell carcinoma thought to be cured)
- Chronic renal, hepatic, or pulmonary disease condition that could interfere with the absorption of the study drug (e.g., surgical resection of significant proportions of the stomach or bowel, gastric bypass, gastric banding, irritable bowel syndrome, inflammatory bowel disease)
- History of known Clostridium difficile infection
- Blood donation within the previous 6 weeks
- History of cardiac rhythm abnormality including Wolff/Parkinson/White syndrome
- History of prolonged QT interval
- History of allergy or photosensitivity to fluoroquinolones
- Prolongation of QTcF interval (i.e., confirmed QTcF interval of 450 milliseconds or greater)
- Clinically significant abnormal 12 lead electrocardiogram at screening in the judgment of the investigator, or based on the formal ECG reading; history of any cardiac abnormalities, including conduction abnormalities such as Wolff-Parkinson-White, dysrhythmias, or coronary artery disease
Laboratory abnormalities at Screening outside of the ranges given below. Note, if one or more screening laboratory values are outside the acceptable range on the initial screen, the abnormal test(s) may be repeated once from a single blood draw:
- Serum creatinine (<1.1 x ULN),
- Hemoglobin (11.0-17.5g/dL),
Platelet count (125,000-450,000mm^3),
- Absolute neutrophil count (>1300 mm^3),
- Aspartate aminotransferase (AST, </=1.2 x ULN),
- Alanine aminotransferase (ALT, </=1.2 x ULN),
- Proteinuria greater than trace (spot urine) and/or hematuria greater than trace.
- Positive serology results for HIV, HBsAg, or HCV antibodies
- Positive urine drug screen for cannabinoids, cocaine, amphetamines, opiates, benzodiazepine, barbiturates, and/or PCP.
- Febrile illness with temperature documented >38 degrees C within 7 days of dosing.
- Pregnancy or breastfeeding
- Known allergic reactions to study drug components, including ingredients present in the formulation.
- Treatment with another investigational drug within 30 days of dosing.
- Lack of ability to fully understand the informed consent. This will be determined by the recruiter/interviewer after explaining the consent and observing the subject reading the consent.
- Ingestion of prescription medications, over-the-counter medicines, grapefruit juice, or specific supplements in the week prior to study enrollment and during the course of the study that, in the judgment of the PI could affect the metabolism of the study drug or safety of the participant (see Concomitant Medications, Section 6.6).
- Use of any form of tobacco, including cigarette smoking, pipe smoking, or oral tobacco; if a former smoker or tobacco user, the subject must not have used tobacco for 30 days before screening.
- Any specific condition that, in the judgment of the Investigator, precludes participation because it could affect subject safety.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación cruzada
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
---|---|
Experimental: SQ109 450 mg
Single daily dose of oral 450mg SQ109 for 7 days.
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300mg or 450mg of SQ109 administered orally, once daily for 7 days.
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Comparador activo: Moxifloxacin
Single daily dose of oral 400mg moxifloxacin for 7 days followed by 7 days washout period.
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400mg of moxifloxacin (positive control) administered orally, once daily for 7 days.
|
Comparador de placebos: SQ109 Placebo
Single daily dose of oral SQ109 placebo for 7 days followed by 7 days washout period.
|
Placebo is a round, coated, yellow, unscored tablet.
SQ109 Placebo administered orally, once daily for 7 days.
|
Experimental: SQ109 300 mg
Single daily dose of oral 300mg SQ109 for 7 days followed by 7 days washout period.
|
300mg or 450mg of SQ109 administered orally, once daily for 7 days.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
---|---|
Solicited and unsolicited adverse events, including symptoms, physical findings, laboratory testing, holter monitor and ECG changes for 300mg/day SQ109
Periodo de tiempo: Days 1-7 of each dosing period and 30 days after last dosing period.
|
Days 1-7 of each dosing period and 30 days after last dosing period.
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Electrocardiogram and holter monitor data (QTc, T wave forms, QRS, RR and PR intervals) for 300mg/day SQ109
Periodo de tiempo: Days 1-7 of each dosing period and 30 days after last dosing period.
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Days 1-7 of each dosing period and 30 days after last dosing period.
|
Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
---|---|
Solicited and unsolicited adverse events, including symptoms, physical findings, laboratory testing, holter monitor and ECG changes for 450mg/day SQ109
Periodo de tiempo: Days 1-7 of each dosing period and 30 days after last dosing period.
|
Days 1-7 of each dosing period and 30 days after last dosing period.
|
Pharmacokinetics of SQ109 at doses of 300 or 450mg/day; AUC0-, (Cmax), time to maximum concentration (Tmax), elimination rate constant, elimination half-life, clearance, volume of distribution, and urinary excretion
Periodo de tiempo: Day 1 and Day 6 of each dosing period
|
Day 1 and Day 6 of each dosing period
|
Electrocardiogram and holter monitor data (QTc, T wave forms, QRS, RR and PR intervals) for 450mg/day SQ109
Periodo de tiempo: Days 1-7 of each dosing period and 30 days after last dosing period.
|
Days 1-7 of each dosing period and 30 days after last dosing period.
|
Colaboradores e Investigadores
Fechas de registro del estudio
Fechas importantes del estudio
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Infecciones
- Infecciones bacterianas
- Infecciones bacterianas y micosis
- Infecciones por bacterias grampositivas
- Infecciones por Actinomycetales
- Infecciones por micobacterias
- Tuberculosis
- Mecanismos moleculares de acción farmacológica
- Agentes antiinfecciosos
- Inhibidores de enzimas
- Agentes antineoplásicos
- Inhibidores de la topoisomerasa II
- Inhibidores de la topoisomerasa
- Agentes antibacterianos
- Moxifloxacino
Otros números de identificación del estudio
- 11-0079
- HHSN272200800026C
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. .
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