Human Absorption, Distribution, Metabolism, and Excretion Study of [14C]Adavosertib - ADME

Study identifier:D601HC00004

ClinicalTrials.gov identifier:NCT05008913

EudraCT identifier:N/A

CTIS identifier:N/A

Terminated/Withdrawn

Official Title

A Phase I, Open-Label, Non-Randomised Study of the Absorption, Distribution, Metabolism, and Excretion of Adavosertib After a Single Oral Dose of [14C]Adavosertib to Patients with Advanced Solid Tumours

Medical condition

Advanced Solid Tumors

Phase

Phase 1

Healthy volunteers

Study drug

[14C]Adavosertib

Sex

All

Actual Enrollment

Study type

Interventional

Age

18 Years - 130 Years

Date

Study Start Date: 01 Oct 2021

Primary Completion Date: 14 Oct 2021

Study Completion Date: 16 Nov 2021

Study design

Allocation: Non-randomized
Endpoint Classification: -
Intervention Model: Single Group Assignment
Masking: -
Primary Purpose: Other

Verification:

Verified 01 Mar 2023 by AstraZeneca

Collaborators

PAREXEL

Inclusion and exclusion criteria

Inclusion Criteria

1.Patient must be ≥ 18 years of age.
2.Histologically or cytologically documented, locally advanced or metastatic solid tumour, excluding lymphoma, for which standard therapy does not exist or has proven ineffective or intolerable.
3.Eastern Cooperative Oncology Group performance status score of 0 to 1.
4.Life expectancy ≥ 12 weeks.
5.Patients must have normal organ and marrow function at baseline, within 7 days prior to study drug administration.
6.Able and willing to stay in hospital for approximately 9 days (first patient; to be evaluated and possibly adjusted for subsequent patients) for the collection of samples following a single oral dose of [14C]-adavosertib.
7.Body weight within 50-100 kg and BMI within the range 18-30 kg/m^2 (inclusive).
8.Regular bowel movements (i.e., on average production of at least 1 faeces per day).
9.Males and females of childbearing potential who agree to use contraceptive measures consistent with local regulations for clinical studies.

Exclusion Criteria

1.Persistent toxicities (Common Terminology Criteria for Adverse Events [CTCAE] Grade > 2) caused by previous anticancer therapy, excluding alopecia and CTCAE Grade 2 peripheral neuropathy.
2.Refractory nausea and vomiting, chronic gastrointestinal disease, inability to swallow the formulated product, or previous significant bowel resection that would preclude adequate absorption, distribution, metabolism, or excretion of 14C-adavosertib oral solution.
3.Patients who have participated in another absorption, distribution, metabolism and excretion study within 1 year prior to screening.
4.Any significant cardiac diseases currently or within the last 6 months such as:
(a) unstable angina pectoris
(b) acute myocardial infarction, congestive heart failure
(c) conduction abnormality not controlled with pacemaker or medication
(d) significant ventricular or supraventricular arrhythmias
5.Any of the following: History or current evidence of congenital long QT syndrome; concomitant medications known to prolong QT
interval or history of medication-related QT prolongation.
6.Known to have tested positive for human immunodeficiency virus or active tuberculosis infection.
7.Known active hepatitis infection, positive hepatitis C antibody, hepatitis B virus surface antigen or hepatitis B virus core antibody, at screening.
8.Any evidence of diseases (such as severe or uncontrolled systemic diseases, including uncontrolled hypertension, renal transplant, active infections, and active bleeding diseases) which prohibit participating in the study.
9.Spinal cord compression or brain metastases unless asymptomatic, stable, and not requiring steroids for at least 4 weeks prior to start of study intervention.
10.Use of an anti-cancer treatment drug ≤ 21 days (≤ 6 weeks for nitroureas or mitomycin C) or use of an investigational product within 5 half-lives prior to the first dose of adavosertib.
11.Patient uses drugs that are sensitive to CYP3A4 substrates or CYP3A4 substrates with a narrow therapeutic index, or are moderate to strong inhibitors/inducers of CYP3A4 which cannot be discontinued 2 weeks or 5 halflives (whichever is longer) prior to Day 1 of dosing.
12.Receipt of live virus and live bacterial vaccines whilst the patient is receiving the study intervention and during the 30-day follow-up period. Inactivated flu vaccines are permitted.
13.Any known hypersensitivity or contraindication to the components of the study intervention adavosertib.
14.Currently pregnant (confirmed with positive pregnancy test) or breast feeding.

No locations available

Arms	Assigned Interventions
Experimental: [14C]Adavosertib Patients will receive a single administration of [14C]adavosertib as an oral solution on Day 1.	-

Documents available

CSR_synopsis
Download
Trial Results Summaries
Available here

Contacts

Contact

AstraZeneca Clinical Study Information Center

1-877-240-9479

[email protected]