Un estudio que proporciona acceso al tratamiento en participantes con hipertensión pulmonar que completan un estudio para padres y no tienen otra opción (PLATYPUS)
Un estudio prospectivo, de etiqueta abierta, de plataforma para el seguimiento a largo plazo de los participantes que utilizan la intervención del estudio en estudios de padres con hipertensión pulmonar
The purpose of the study is to enable participants with pulmonary hypertension (PH) currently treated with study intervention(s) in a clinical study (parent studies [NCT03422328, NCT03904693,NCT04565990, NCT02932410, NCT03492177, and NCT04175600]), to continue to benefit from the intervention after closure of the parent study in case they have no alternative means of access to the study intervention. This study will allow assessment of the long-term safety of each study intervention.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 3
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Study Contact
- Número de teléfono: 844-434-4210
- Correo electrónico: Participate-In-This-Study1@its.jnj.com
Ubicaciones de estudio
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Minsk, Bielorrusia, 220036
- Reclutamiento
- The Republican Scientific-Practical Center ''Cardiology''
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Minsk, Bielorrusia
- Terminado
- Minsk Regional Clinical Hospital Of The Red Banner Of Labor
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Sofia, Bulgaria, 1750
- Reclutamiento
- University Multiprofile Hospital for Active Treatment- UMHAT Sveta Anna AD
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Leuven, Bélgica, 3000
- Terminado
- UZ Leuven
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Daejeon, Corea del Sur, 35015
- Reclutamiento
- Chungnam National University Hospital
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Incheon, Corea del Sur, 21565
- Reclutamiento
- Gachon University Gil Medical Center
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Seoul, Corea del Sur, 05505
- Reclutamiento
- Asan Medical Center
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Seoul, Corea del Sur, 03080
- Reclutamiento
- Seoul National University Hospital
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Seoul, Corea del Sur, 06351
- Reclutamiento
- Samsung Medical Center
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Seoul, Corea del Sur, 06591
- Terminado
- The Catholic University of Korea Seoul St Marys Hospital
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Seoul, Corea del Sur, 03080
- Reclutamiento
- Seoul National University Hospital 1
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Budapest, Hungría, 1096
- Reclutamiento
- Gottsegen György Országos Kardiológiai Intézet
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Bialystok, Polonia, 15 276
- Reclutamiento
- Klinika Kardiologii Z Oddzialem Intensywnego Nadzoru Kardiologicznego UM W Bialymstoku
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Bydgoszcz, Polonia, 85-168
- Terminado
- Szpital Uniwersytecki nr 2 im dr Jana Biziela w Bydgoszczy, Klinika Kardiologii
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Katowice, Polonia, 40 635
- Reclutamiento
- SPSK nr 7 SUM w Katowicach Gornoslaskie Centrum Medyczne im Prof Leszka Gieca
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Lodz, Polonia, 91 347
- Terminado
- Oddzial Kardiologii Wojewodzki Szpital Specjalistyczny im W Bieganskiego
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Lublin, Polonia, 20 718
- Terminado
- Wojewodzki Szpital Specjalistyczny im Stefana Kardynala Wyszynskiego SPZOZ
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Szczecin, Polonia, 70 111
- Terminado
- SPSK2 PUM Klinika Kardiologii
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Wroclaw, Polonia, 51 124
- Terminado
- Wojewodzki Szpital Specjalist Osrodek Badawczo Rozwojowy
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Wroclaw, Polonia, 51 124
- Reclutamiento
- Wojewodzki Szpital Specjalistyczny we Wroclawiu
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Beijing, Porcelana, 100029
- Reclutamiento
- Beijing Anzhen Hospital
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Beijing, Porcelana, 100029
- Reclutamiento
- Beijing Anzhen Hospital 1
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Changsha, Porcelana, 410011
- Reclutamiento
- The Second Xiangya Hospital of Central South Hospital
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Nanjing, Porcelana
- Reclutamiento
- Jiangsu Province Hospital
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Qingdao, Porcelana, 266035
- Reclutamiento
- Qingdao Women and Children's Hospital
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Shanghai, Porcelana, 200062
- Reclutamiento
- Childrens Hospital of Shanghai
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Xi'an, Porcelana, 710061
- Reclutamiento
- The First Affiliated Hospital of Xian Jiaotong University
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Kemerovo, Rusia, 650002
- Terminado
- Scientific and Research Institution of Cardiovascular Diseases Complex Problems
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Novosibirsk, Rusia, 630055
- Reclutamiento
- E.Meshalkin National Medical Research Center of the Ministry of Health of the Russian Federation
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Saint Petersburg, Rusia, 197341
- Terminado
- Federal State Budgetary Institution
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Tomsk, Rusia, 634012
- Terminado
- Institute of Cardiology of Tomsk National Research Medical Center of Rus Academy of Sciences
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Tyumen, Rusia, 625000
- Reclutamiento
- Regional Clinical Hospital No1
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Durban, Sudáfrica, 4001
- Terminado
- Abdullah, IA
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Lenasia, Sudáfrica, 1820
- Reclutamiento
- Dr Kalla
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Chiang Mai, Tailandia, 50200
- Reclutamiento
- Maharaj Nakorn Chiang Mai hospital Faculty of Medicine
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Kaohsiung City, Taiwán, 813
- Reclutamiento
- Kaohsiung Veterans General Hospital
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Tainan, Taiwán, 704
- Reclutamiento
- National Cheng Kung University Hospital
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Taipei, Taiwán, 100
- Reclutamiento
- National Taiwan University Hospital
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Taipei, Taiwán, 112
- Reclutamiento
- Taipei Veterans General Hospital
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Taoyuan, Taiwán, 333
- Reclutamiento
- Chang-Gung Memorial Hospital, LinKou Branch
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Dnipro, Ucrania
- Terminado
- Municipal Inst. Of Dnipropetrovsk Region. Council
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Kyiv, Ucrania, 03680
- Terminado
- State Institute Of Phthisiology And Pulmonology N.A. F.G. Yanovskiy Of Ams Ukraine
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Hanoi, Vietnam
- Reclutamiento
- Hanoi Medical University Hospital
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Hanoi, Vietnam
- Reclutamiento
- Hanoi Heart Hospital
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Ho Chi Minh City, Vietnam
- Reclutamiento
- Children's Hospital 1
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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:
- Participant must sign an informed consent form (ICF) (or their legally designated representative must sign) indicating that participant understands the purpose of, and procedures required for, the study and is willing to participate in the study
- Participant treated with oral macitentan or selexipag or fixed dose combination (FDC) of macitentan 10 milligrams (mg) and tadalafil 40 mg at the end of a sponsor parent study and: a) the indication of the parent study is included in the intervention-specific appendices (ISA) (pulmonary arterial hypertension [PAH]; b) participant has completed the parent study; c) no alternative means of access to study intervention (or equivalent approved therapy) have been identified; d) participant may continue to benefit from treatment with the study intervention; e) Participant is at least 18 years old for macitentan/tadalafil FDC, and at least 2 years old for macitentan or selexipag
- A female participant of childbearing potential must: a) have a negative urine or serum pregnancy test prior to first intake of study intervention; b) agree to perform monthly urine pregnancy test up to the end of the safety follow-up period; c) If heterosexually active, agree to follow contraceptive methods until 30 days after the last intake of the study intervention. For pediatric female participants: It is the responsibility of the investigator to ensure appropriate counselling, including consultation with a specialist (if needed), to the participant and/or parent(s)/ legally designated representative (LDR)(s) on the acceptable method of contraception
Exclusion Criteria:
General:
- Participants prematurely discontinued from the study intervention in their parent study
- Female participant being pregnant, or breastfeeding, or planning to become pregnant while enrolled in this study
- Planned or current treatment with another investigational treatment
Macitentan-specific:
- Known allergies, hypersensitivity, or intolerance to macitentan or its excipients
- Hemoglobin less than (<) 80 grams per liter (g/L)
- Serum aspartate (AST) and/or alanine aminotransferases (ALT) greater than (>) 3* upper limit of normal (ULN)
- Known and documented severe hepatic impairment that is, Child-Pugh Class C. For participants with hepatic impairment, Child-Pugh Class (Child-Pugh score) should be fully assessed and documented in the source documents at screening
Selexipag-specific:
- Known allergies, hypersensitivity, or intolerance to selexipag or its excipients
- Suspected or known pulmonary veno-occlusive disease (PVOD)
- Uncontrolled thyroid disease
- Severe coronary heart disease or unstable angina, myocardial infarction within the last 6 months, decompensated cardiac failure (if not under close medical supervision), severe arrhythmia, cerebrovascular events (for example, transient ischemic attack, stroke) within the last 3 months, or congenital or acquired valvular defects with clinically relevant myocardial function disorders not related to pulmonary hypertension (PH)
- Known and documented severe hepatic impairment that is, Child-Pugh Class C. For participants with hepatic impairment, Child-Pugh Class (Child-Pugh score) should be fully assessed and documented in the source documents at screening
- Children only: (a) Current suspicion of intussusception or ileus or gastrointestinal obstruction, per the investigator's judgment; (b) hemoglobin or hematocrit <75 percent (%) of the lower limit of normal range
Macitentan/tadalafil FDC-specific:
- Known allergies, hypersensitivity, or intolerance to macitentan or tadalafil or their excipients
- Hemoglobin <80 g/L
- Serum aspartate (AST) and/or alanine aminotransferases (ALT) >3* ULN range
- Known and documented severe hepatic impairment that is, Child-Pugh Class C. For participants with hepatic impairment, Child-Pugh Class should be fully assessed and documented in the source documents at screening
- Severe renal impairment (estimated glomerular filtration rate [eGF]/creatinine clearance <30 milliliter per minute [mL/min])
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Macitentan
Participants who have completed a parent study, benefit from their study intervention maintenance and have no adequate alternative local treatment option will be enrolled in this study and will continue to receive study drug macitentan orally during the course of the study. For adult participants study visits will be scheduled every 6 months and for pediatric participants study visits will be scheduled every 3 months. The study includes on-site visits to collect efficacy and safety information until participant discontinuation/withdrawal, or the respective study intervention is made commercially available in the country/territory or an equivalent approved therapy becomes available, or the sponsor decides to terminate the study prematurely. |
Adult participants will receive oral dose of macitentan 10 milligrams (mg) tablet once daily. Children greater than or equal to (>=) 2 year to less than (<) 18 years will be given an oral macitentan dose tailored to their body weight, ensuring an equivalent level of systemic exposure as in adults.
Otros nombres:
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Experimental: Selexipag
Participants who have completed a parent study, benefit from their study intervention maintenance and have no adequate alternative local treatment option will be enrolled in this study and will continue to receive study drug selexipag orally during the course of the study. Study visits are scheduled every 6 months to collect efficacy and safety information until participant discontinuation/withdrawal, or the respective study intervention is made commercially available in the country/territory or an equivalent approved therapy becomes available, or the sponsor decides to terminate the study prematurely. |
Adult Participant will receive oral dose of selexipag tablet twice daily at the dose strength corresponding to their maintenance dose at the end of their parent study. Available strengths: 200, 400, 600, 800, 1000, 1200, 1400 and 1600 micrograms (µg). Children with body weight category of >=50 kg will use the tablets at the required dose strength as described for adults. Children with a body weight < 50 kg will receive tablets for pediatric use (dose strengths: 100 and 150 mcg), twice daily to enable continuation of individually maximum tolerated dose of selexipag according to their body weight category.
Otros nombres:
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Experimental: Macitentan/Tadalafil FDC
Participants who have completed a parent study, benefit from their study intervention maintenance and have no adequate alternative local treatment option will be enrolled in this study and will continue to receive drug Macitentan and Tadalafil fixed dose combination (FDC) orally during the course of the study. Study visits are scheduled every 6 months to collect efficacy and safety information until participant discontinuation/withdrawal, or the respective study intervention is made commercially available in the country/territory or an equivalent approved therapy becomes available, or the sponsor decides to terminate the study prematurely. |
Participants will receive oral FDC of macitentan 10 mg and tadalafil 40 mg once daily during the course of the study as already received in the parent studies.
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Frequency of Treatment Emergent Adverse Events (TEAEs)
Periodo de tiempo: Baseline until End of Study (EOS) (up to 84 months)
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An adverse event (AE) is any untoward medical occurrence in a clinical study participant administered a pharmaceutical (investigational or non-investigational) product. An AE does not necessarily have a causal relationship with the intervention. TEAEs are defined as a treatment-emergent AE is any AE temporally associated with the use of study treatment (from start of treatment in the PLATYPUS protocol until 30 days after study treatment discontinuation) whether or not considered by the investigator as related to study treatment. |
Baseline until End of Study (EOS) (up to 84 months)
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Frequency of TEAEs Leading to Discontinuation
Periodo de tiempo: Baseline until EOS (up to 84 months)
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Frequency of TEAEs leading to discontinuation of study intervention will be reported. An AE is any untoward medical occurrence in a clinical study participant administered a pharmaceutical (investigational or non-investigational) product. An AE does not necessarily have a causal relationship with the intervention. TEAEs are defined as a treatment-emergent AE is any AE temporally associated with the use of study treatment (from start of treatment in the PLATYPUS protocol until 30 days after study treatment discontinuation) whether or not considered by the investigator as related to study treatment. |
Baseline until EOS (up to 84 months)
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Frequency of Serious Adverse Events (SAEs)
Periodo de tiempo: Baseline until EOS (up to 84 months)
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SAE is any untoward medical occurrence that at any dose results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, is a suspected transmission of any infectious agent via a medicinal product and is medically important. |
Baseline until EOS (up to 84 months)
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Frequency of Deaths
Periodo de tiempo: Baseline until EOS (up to 84 months)
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Frequency of deaths will be reported. |
Baseline until EOS (up to 84 months)
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Director de estudio: Actelion Pharmaceuticals Ltd Clinical Trial, Actelion
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
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
Otros números de identificación del estudio
- CR109121
- 2021-002297-11 (Número EudraCT)
- NOPRODPAPUH3001 (Otro identificador: Janssen Research & Development, LLC)
- 2023-506791-27-00 (Identificador de registro: EUCT number)
- 2023 (Subvención/contrato del NIH de EE. UU.)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
The data sharing policy of Johnson & Johnson Innovative Medicine is available at innovativemedicine.jnj.com/our-innovation/clinical-trials/transparency. As noted on this site, requests for access to the study data can be submitted through Yale Open Data Access (YODA) Project site at yoda.yale.edu
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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. .