Long-term Safety Study of Chronocort in the Treatment of Participants With Congenital Adrenal Hyperplasia

Overview

Información sobre este estudio

The purpose of this study is to evaluate the long-term safety and tolerability of Chronocort in participants aged 16 years and over when used as treatment for Congenital Adrenal Hyperplasia (CAH).

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

- Participants with Congenital adrenal hyperplasia (CAH), in eligible countries who have
successfully completed one of the specified previous Chronocort studies (DIUR-006 or
DIUR-014).

- Participants who are capable of giving signed informed consent/assent.

Exclusion Criteria:

- Participants with clinical or biochemical evidence of hepatic or renal disease; e.g.,
creatinine > 2 times the upper limit of normal (ULN) or elevated liver function tests
(alanine aminotransferase [ALT] or aspartate aminotransferase [AST] > 2 times the ULN).

- Participants with a history of malignancy (other than basal cell carcinoma
successfully treated > 26 weeks prior to entry into the study).

- Participants with a history of bilateral adrenalectomy.

- Participants with any other significant medical or psychiatric conditions that in the
opinion of the Investigator would preclude participation in the study.

- Participants with a co-morbid condition requiring daily administration of a medication
or consumption of any material that interferes with the metabolism of glucocorticoids.

- Participants on regular daily inhaled, topical, nasal, or oral steroids for any
indication other than CAH.

- Participants anticipating regular prophylactic use of additional steroids e.g., for
strenuous exercise.

- Participation in another clinical study of an investigational or licensed drug or
device within 3 months prior to inclusion in this study, except for another clinical
study with the current formulation of Chronocort.

- Females who are pregnant or lactating.

- Participants, who in the opinion of the Investigator, will be unable to comply with
the requirements of the protocol.

- Participants who routinely work night shifts and so do not sleep during the usual
night-time hours.

- Participants with a body weight of 50 kg or less.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 5/1/23. Questions regarding updates should be directed to the study team contact.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Irina Bancos, M.D., M.S.

Cerrado para la inscripción

Contact information:

Cayse Powell M.D.

(507) 538-5193

Powell.Cayse@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20552884

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