Status:
COMPLETED
Capivasertib China PK Study
Lead Sponsor:
AstraZeneca
Conditions:
Advanced Solid Tumours
Eligibility:
All Genders
18-130 years
Phase:
PHASE1
Brief Summary
This is an open-label, 2-part Phase I study to assess the PK, safety and tolerability of capivasertib as monotherapy and in combination with paclitaxel in Chinese participants with advanced solid tumo...
Detailed Description
A Phase I study is designed to assess the PK, safety and tolerability of single-dose and multiple-dose capivasertib as monotherapy (Part A) and in combination with paclitaxel (Part B) in approximately...
Eligibility Criteria
Inclusion
- Key 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:
- Mean resting corrected QT interval (QTc) \>470 msec obtained from 3 consecutive ECGs
- 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:
- Participants with diabetes mellitus type I or diabetes mellitus type II requiring insulin treatment
- 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.
Exclusion
Key Trial Info
Start Date :
February 22 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 29 2022
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT04742036
Start Date
February 22 2021
End Date
July 29 2022
Last Update
August 19 2022
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Research Site
Shanghai, China, 200032