Pharmacokinetic (PK), Pharmacodynamic (PD) and Tolerability of Osilodrostat in Pediatric Patients With Cushing's Syndrome

NCT ID: NCT03708900

Last Updated: 2025-11-20

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-04-28
• Study Completion Date: 2025-11-21

Brief Summary

Multicenter, open-label, non-comparative study to evaluate the pharmacokinetics, pharmacodynamics, and tolerability of osilodrostat in children and adolescent patients with Cushing's syndrome.

Detailed Description

The period 1 study duration will be 12 weeks. The study will include a screening period of up to 4 weeks prior to Day 0 (baseline) (to allow for an adequate washout period from any medications that may modify cortisol levels). All subjects being treated with osilodrostat at 12 weeks and obtaining benefit from therapy, per investigator judgment, will be offered participation in an optional 9-month extension period, during which assessment of the PD activity and safety/tolerability of osilodrostat will be done. Patients who do not enter the optional extension period will have a safety follow up visit 4 weeks later.

Conditions

Cushing Syndrome

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

LCI699 (osilodrostat)

Subjects with cushing's syndrome taking LCI699 (osilodrostat)

Group Type: EXPERIMENTAL

LCI699

Intervention Type: DRUG

osilodrostat (LCI699) is in the form of tablets 1 milligram (mg), 5 mg, and 10mg or in form of capsules 0.1 mg, 0.2 mg, 0.5 mg, 1 mg or 5 mg, both the formulations for oral administration

Interventions

LCI699

osilodrostat (LCI699) is in the form of tablets 1 milligram (mg), 5 mg, and 10mg or in form of capsules 0.1 mg, 0.2 mg, 0.5 mg, 1 mg or 5 mg, both the formulations for oral administration

Intervention Type: DRUG

Other Intervention Names

osilodrostat

Eligibility Criteria

Inclusion Criteria

1. Male and female children and adolescents from 2 to < 18 years of age with Cushing's syndrome of endogenous origin: Who have failed surgery (or) who are awaiting surgery (or) for whom surgery is not an immediate option. For patients who are awaiting surgery, the study treatment could be less than 12 weeks.

2. Patients must weigh > 10 kg.

3. The diagnosis of Cushing's syndrome must be confirmed by each of the following:

3a) The clinical criterion of decreasing growth percentiles with increasing weight (as evidenced by the presence of a contrast in height and BMI SD scores, for example a SDS < 0 and BMI SDS > 0, or a strong clinical suspicion of Cushing's syndrome, such as photographic evidence of a change in facial appearance); 3b) Abnormal low-dose (0.5 mg Q6h x 48 hours, or overnight 15mcg/kg [max 1 mg]) dexamethasone suppression test, defined as plasma cortisol levels > 1.8 mcg/dl, at time point 48 hours (0.5 mg Q6h x 48 hours) or 9 to 12 hours (overnight 15mcg/kg [max 1 mg]) after the first dose of dexamethasone; (OR) Midnight serum cortisol levels > ULN, assessed while the patient is sleeping and after pre-cannulation (OR) two samples of late-night salivary cortisol greater than ULN for the assay. 3c)Two 24-hour urinary free cortisol values > 1.3 x ULN;

4. Able to swallow study drug tablets (not crushed or split) or the content of the capsules mixed with water.

5. Parents or legal guardians able to provide consent/assent.

Exclusion Criteria

1. Patients with macroadenoma complicated by compressive symptoms (requiring urgent surgical intervention) or at high risk for compressive symptoms due to mass effect of tumor (concern of corticotroph tumor progression).

2. Insufficient washout period from any other medication used to lower cortisol levels (5 half-lives of any drug).

3. Use of other investigational drugs at the time of enrollment, or within 30 days, or prior to completion of a wash-out duration that is at least 5 half- lives of the drug, at the time of enrollment, whichever is longer. Local regulations may require a longer wash-out period or specify other limitations for participation in an investigational trial, in which case they will be applicable as well.

4. History of hypersensitivity to drugs of the same or similar chemical classes as osilodrostat.

5. History of malignancy of any organ system (other than localized basal cell carcinoma of the skin), treated or untreated, within the past 5 years, regardless of whether there is evidence of local recurrence or metastases.

6. Patients with moderate to severe renal impairment (estimated GFR < 60 mL/min by the Creatinine-based "Bedside Schwartz" equation).

7. Patients with serum ALT and/or AST > 3 x ULN, or total bilirubin > 1.5 x ULN.

8. History of thrombosis.

9. Patients with risk factors for QTc prolongation or Torsade de Pointes, including: 9a) patients with a baseline QTcF > 450 ms 9b) personal or family history of long QT syndrome 9c) concomitant medications known to prolong the QT interval 9d) patients with hypokalemia, hypocalcaemia, or hypomagnesaemia, if not corrected before pre-dose Day 0. In case of uncorrected hypokalemia (<3.5 mEq/L), the screening period may be used to correct hypokalemia prior to starting study drug. Use of potassium supplements and/or mineralocorticoid antagonists is permitted during the study. 9e) Patients with a history of significant cardiovascular disease (based on the opinion of the investigator) such as: structural cardiovascular abnormalities, arrhythmia,

10. Hypertensive patients with uncontrolled blood pressure defined as SBP > 150 and/or DBP > 100 or not optimally treated for hypertension as judged by the investigator.

11. Patients who have undergone any major surgery within 1 month.

12. Patients who have undergone trans-sphenoidal pituitary surgery within 6 weeks prior to screening are not eligible, unless they have clear evidence of persistent hypercortisolism or persistent biochemical changes consistent with Cushing's syndrome.

13. Use of or anticipated use of systemic glucocorticoid medications 1 month prior to screening.

14. Uncontrolled hypothyroidism as evidenced by Free T4 < 0.8 ng/dl.

15. Uncontrolled hyper thyroidism.

16. Diabetic patients with poorly controlled diabetes as evidenced by HbA1c > 8.5 % or not optimally treated for diabetes mellitus as judged by the investigator.

17. Positive pregnancy test in females of childbearing potential.

18. Female patients of childbearing potential who do not agree to use highly effective birth control methods .

19. Pregnant or nursing (lactating) women.

20. Any medical condition that would, in the investigator's judgment, prevent the patient's participation in the clinical study due to safety concerns or compliance with clinical study procedures. Any severe, acute, or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or study treatment administration or that may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for the study.

21. Use of concomitant prohibited medications

• Minimum Eligible Age: 2 Years
• Maximum Eligible Age: 17 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

RECORDATI GROUP

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Recordati AG

Role: STUDY_DIRECTOR

Recordati AG

Locations

University of California San Francisco UCSF

San Francisco, California, United States

Site Status: RECRUITING

National Institute of Child Health and Human Development

Bethesda, Maryland, United States

Site Status: COMPLETED

UZ Brussel

Jette, Brussels Capital, Belgium

Site Status: COMPLETED

Multiprofile Hospital for Active Treatment Sveta Marina EAD

Varna, , Bulgaria

Site Status: WITHDRAWN

Hospital Necker Enfants Malades

Paris, , France

Site Status: COMPLETED

Robert Debre Hospital

Paris, , France

Site Status: COMPLETED

CHU Bicetre APHP Paris Saclay

Paris, , France

Site Status: COMPLETED

Aziendal Ospedaliero Universitaria Pisana Presidio Ospedale di Cisanello

Pisa, PI, Italy

Site Status: COMPLETED

Ospedale Bambino Gesu

Roma, , Italy

Site Status: COMPLETED

University Clinical Center Ljubljana

Ljubljana, , Slovenia

Site Status: WITHDRAWN

Alder Hey Childrens NHS Foundation Trust

Liverpool, , United Kingdom

Site Status: WITHDRAWN

The Royal London Childrens Hospital

London, , United Kingdom

Site Status: WITHDRAWN

Countries

United States; Belgium; Bulgaria; France; Italy; Slovenia; United Kingdom

Central Contacts

Recordati

Role: CONTACT

casi.m@recordati.it

+39 0248787456

Recordati

Role: CONTACT

+4161 205 61 00

Facility Contacts

Maya Lodish

Role: primary

maya.lodish@ucsf.edu

415-476-3310

Other Identifiers

2018-001522-25

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

CLCI699C2203

Identifier Type: -

Identifier Source: org_study_id