Study of ORIC-101 in Healthy Adult Subjects

Healthy Volunteers Clinical Trial

Official title:

A Phase 1 Single-ascending Dose Study of the Oral Glucocorticoid Receptor Antagonist ORIC-101 in Healthy Adult Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03324555
• Other study ID #: ORIC-GR-17001
• Status: Completed
• Phase: Phase 1
• First received: October 25, 2017
• Last updated: April 3, 2018
• Start date: October 19, 2017
• Est. completion date: December 18, 2017

Study information

• Verified date: April 2018
• Source: Oric Pharmaceuticals
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

ORIC-GR-17001 is an open-label, single center, non-randomized, single ascending dose study in healthy male subjects and healthy female subjects of non-child bearing potential. In this study, ORIC-101 will be administered as single-ascending oral doses. The primary objective is to characterize the safety and tolerability of oral ORIC-101.

Description:

This is an open-label, single center, non-randomized, single ascending dose study in healthy male subjects and healthy female subjects of non-child bearing potential.

Subjects will receive a single administration of ORIC-101 oral suspension on a single occasion and will be followed in the clinic for at least 96 hours post-dose. Total subject participation will be approximately 5 weeks from screening until discharge from the study.

The primary objective of the study is to characterize the safety and tolerability of oral ORIC-101 administered as a single dose in adult healthy subjects. The secondary objective of the study is to evaluate the pharmacokinetics of ORIC-101 and its metabolites M1 and M2. The exploratory objective of the study is to assess the pharmacodynamics of ORIC-101 by measurement of serum and urine levels of cortisol and other biological markers in healthy subjects

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: December 18, 2017
• Est. primary completion date: December 18, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Healthy males or healthy females of non-child bearing potential

2. Age 18 to 55 years, inclusive

3. Weighs more than 50 kilograms (kg), and less than 120 kg, with a body mass index of 18.0 to 32.0 kg/meters squared

Exclusion Criteria:

1. Subjects who have received any investigational medicinal product (IMP) in a clinical research study within 5 half-lives or within 45 days prior to first dose. However, in no event, shall the time between last receipt of IMP and first dose be less than 30 days

2. History of any drug or alcohol abuse in the past 2 years

3. Current smokers and those who have smoked within the last 12 months

4. Females of childbearing potential (female subjects must have a negative pregnancy test). A woman is considered of childbearing potential unless she is permanently sterile (hysterectomy, bilateral salpingectomy, tubal ligation or bilateral oophorectomy) or is postmenopausal (had no menses for 12 months without an alternative medical cause and a serum follicle-stimulating hormone [FSH] concentration =40 international units per litre (IU/L))

5. Women with a history of unexplained vaginal bleeding or endometrial hyperplasia with atypia or endometrial carcinoma

6. Current disease requiring treatment with systemic corticosteroids.

7. Serious adverse reaction or serious hypersensitivity to mifepristone, or any other drug, or the formulation excipients

Related Conditions & MeSH terms

• Healthy Volunteers

Intervention

Drug:
• ORIC-101
Oral suspension

Locations

Country	Name	City	State
United States	Research Center	Miami	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Oric Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and tolerability, as assessed by incidence and severity of adverse events.		96 hours post-dose
Secondary	Pharmacokinetics, as assessed by time of observed maximum concentration (Tmax)		96 hours post-dose
Secondary	Pharmacokinetics, as assessed by maximum concentration observed (Cmax)		96 hours post-dose
Secondary	Pharmacokinetics, as assessed by area under the concentration versus time curve from time 0 to 24 hours post-dose (AUC(0-24))		96 hours post-dose
Secondary	Pharmacokinetics, as assessed by area under the concentration versus time curve from time 0 to last measurable concentration (AUC(0-last))		96 hours post-dose
Secondary	Pharmacokinetics, as assessed by area under the concentration versus time curve from time 0 extrapolated to infinity (AUC(0-inf))		96 hours post-dose