Capivasertib China PK study

Study identifier:D3614C00002

ClinicalTrials.gov identifier:NCT04742036

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Phase I Open-label Study to Assess the Pharmacokinetics, Safety, and Tolerability of Capivasertib Monotherapy and in Combination with Paclitaxel in Chinese Patients with Advanced Solid Tumours.

Medical condition

Advanced Solid Tumours

Phase

Phase 1

Healthy volunteers

Study drug

Capivasertib, Paclitaxel

Sex

All

Actual Enrollment

Study type

Interventional

Age

18 Years - 130 Years

Date

Study Start Date: 22 Feb 2021

Primary Completion Date: 29 Jul 2022

Study Completion Date: 29 Jul 2022

Study design

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

Verification:

Verified 01 Jun 2023 by AstraZeneca

Collaborators

Inclusion and exclusion criteria

Inclusion Criteria

• Participants must have at least 1 lesion, not previously irradiated, that can be measured accurately at baseline as ≥10 mm in the longest diameter (except lymph nodes which must have short axis ≥15 mm) with computer tomography (CT) or magnetic resonance imaging (MRI) which is suitable for accurate repeated measurements, or Lytic or mixed (lytic + sclerotic) bone lesions that can be assessed by CT or MRI in the absence of measurable disease as defined above; patients with sclerotic/osteoblastic bone lesions only in the absence of measurable disease are not eligible.
• Histologically or, where appropriate, cytologically-confirmed malignant solid tumour refractory or resistant to standard therapy and for which no suitable effective standard therapy exists
• Participants must have a life expectancy of ≥12 weeks
• Participants must be eligible for paclitaxel treatment as per local investigator assessment
• ECOG performance status 0-1
• Participants must be on a stable concomitant medication regimen, defined as no changes in medication or in dose within 2 weeks prior to start of capivasertib dosing, except for bisphosphonates, denosumab and corticosteroids, which should be stable for at least 4 weeks prior to start of capivasertib dosing
Key

Exclusion Criteria

• Radiotherapy with a wide field of radiation within 4 weeks before the first dose of study treatment
• Other malignancies within 5 years prior to treatment initiation (except for appropriately treated carcinoma in situ of the cervix, non-melanoma skin carcinoma, or Stage I uterine cancer)
• Participants with any ongoing toxicities (>CTCAE grade 2), with the exception of alopecia, caused by previous cancer therapy
• Past medical history of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis which required steroid treatment, or any evidence of clinically active interstitial lung disease
• Any of the following cardiac criteria at screening:
o Mean resting corrected QT interval (QTc) >470 msec obtained from 3 consecutive ECGs
o Any clinically important abnormalities in rhythm, conduction or morphology of resting ECG (eg, complete left bundle branch block, third-degree heart block)
• Clinically significant abnormalities of glucose metabolism as defined by any of the following at screening:
o Participants with diabetes mellitus type I or diabetes mellitus type II requiring insulin treatment
o glycosylated haemoglobin (HbA1c) ≥8.0% (63.9 mmol/mol)
• Inadequate bone marrow reserve or organ function
• Spinal cord compression or brain metastases unless asymptomatic, treated and stable and not requiring steroids for at least 4 weeks prior to start of study treatment
• Major surgery (excluding placement of vascular access) within 4 weeks of the first dose of study treatment
• Refractory nausea and vomiting, malabsorption syndrome, chronic gastrointestinal diseases, inability to swallow the formulated product or previous significant bowel resection, or other condition that would preclude adequate absorption of capivasertib
• Previous allogeneic bone marrow transplant or solid organ transplant
• Evidence of dementia-altered mental status or any psychiatric condition that would prohibit understanding or rendering of informed consent
• Any other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding that, in the investigator’s opinion, gives reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug, may affect the interpretation of the results, render the patient at high risk from treatment complications or interferes with obtaining informed consent
• Any previous treatment with AKT, PI3K, and/or mTOR inhibitors
• Participation in another clinical study with an IP administered in the last 30 days or 5 half-lives, whichever is longer.

No locations available

Arms	Assigned Interventions
Experimental: capivasertib single-dose and multiple-dose capivasertib as monotherapy (Part A) and then in combination with paclitaxel (Part B)	-

Documents available

Redacted CSR synopsis
Download
Trial Results Summaries
Available here

Contacts

Contact

AstraZeneca Clinical Study Information Center

1-877-240-9479

[email protected]

Investigators

Principal Investigator

Xichun Hu

Department of Medical Oncology, Fudan University Shanghai Cancer Center