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Clinical Trials in the UK / NCT04644068
Active, not recruiting Phase 1/2

Study of AZD5305 as Monotherapy and in Combination With Anti-cancer Agents in Patients With Advanced Solid Malignancies

NCT04644068 · tracked via the Priya Life Science UK tracker
Sponsor
AstraZeneca
Phase
Phase 1/2
Started
2020-11-12
Last updated
2026-08-19

Condition(s) studied

Ovarian CancerBreast CancerPancreatic CancerProstate CancerAdditional Indications Below for Module 4 and 5Non-small Cell Lung CancerColorectal CancerBladder CancerGastric CancerBiliary CancerCervical CancerEndometrial CancerSmall Cell Lung Cancer Only in Module 5

Investigational drug(s) / intervention(s)

AZD5305PaclitaxelCarboplatinT- DxdDato-DXdCamizestrant

AZD5305: Oral PARP inhibitor

Paclitaxel: IV Anti-microtubule agent

Carboplatin: IV Platinum chemotherapeutic

T- Dxd: IV Antibody-drug conjugate

Dato-DXd: IV Antibody-drug conjugate

Camizestrant: Oral SERD Molecule

Study summary

This research is designed to determine if experimental treatment with PARP inhibitor, AZD5305, alone, or in combination with anti-cancer agents is safe, tolerable, and has anti-cancer activity in patients with advanced solid tumors.

Eligibility

Sex
ALL
Min age
18 Years
Max age
130 Years
Healthy volunteers
No
Key Inclusion Criteria: * Age ≥ 18 at the time of screening * Histological or cytological confirmation of advanced malignancy considered to be suitable for study treatment and meeting module specific eligibility criteria.. * Eastern Cooperative Oncology Group Performance status (ECOG PS: 0-2) * Life expectancy ≥ 12 weeks * Progressive cancer at the time of study entry * Patients must have evaluable disease as defined in module-specific criteria for Part A and Part B * Adequate organ and marrow function as defined by the protocol. * For Part B expansion cohorts: Provision of formalin-fixed and paraffin embedded (FFPE) tumour specimen is mandatory, where available, except if stated that it is optional in a specific Module. For Part A: \- Patients may have received up to one prior line of therapy with a PARPi-based regimen (either as a treatment or as maintenance) For Part B: \- Patients must not have received prior therapy with a PARPi-based regimen (either as a treatment or as maintenance). Key Exclusion Criteria: * Treatment with any of the following: 1. Nitrosourea or mitomycin C within 6 weeks of the first dose of study treatment 2. Any investigational agents or study drugs from a previous clinical study within 5 half-lives or 3 weeks (whichever is shorter) of the first dose of study treatment 3. Any other chemotherapy, immunotherapy or anticancer agents within 3 weeks of the first dose of study treatment 4. Any live virus or bacterial vaccine within 28 days of the first dose of study treatment * Concomitant use of medications or herbal supplements known to be cytochrome P450 3A4 (CYP3A4) strong inhibitors or inducers. * Concomitant use of drugs that are known to prolong or shorten QT and have a known risk of Torsades de Pointes. * Receiving continuous corticosteroids at a dose of \>10 mg prednisone/day or equivalent for any reason. * Major surgery within 4 weeks of the first dose of study treatment. * Radiotherapy with a wide field of radiation within 4 weeks or radiotherapy with a limited field of radiation for palliation within 2 weeks of the first dose of study treatment. * Any history of persisting (\> 2 weeks) severe pancytopenia due to any cause * Spinal cord compression or brain metastases unless asymptomatic, treated and stable and not requiring continuous corticosteroids at a dose of \>10mg prednisone/day or equivalent for at least 4 weeks prior to start of study treatment. Patients with leptomeningeal carcinomatosis are excluded. * patient with known predisposition to bleeding (e.g., active peptic ulceration, recent \[within 6 months\] haemorrhagic stroke, proliferative diabetic retinopathy). * Cardiac conditions as defined by the clinical study protocol * Other cardiovascular diseases as defined by any of the following: 1. Symptomatic heart failure, 2. uncontrolled hypertension, 3. hypertensive heart disease with significant left ventricular hypertrophy 4. acute coronary syndrome (ACS)/acute myocardial infarction (AMI), unstable angina pectoris, coronary intervention procedure with percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG) within 6 months. 5. cardiomyopathy of any etiology 6. presence of clinically significant valvular heart disease 7. history of atrial or ventricular arrhythmia requiring treatment; subjects with atrial fibrillation and optimally controlled ventricular rate (\< 100 beats per minute) are permitted. 8. subjects with atrial fibrillation and optimally controlled ventricular rate are permitted 9. transient ischaemic attack, or stroke within 6 months prior to screening 10. patients with symptomatic hypotension at screening * Patients with myelodysplastic syndrome/acute myeloid leukaemia or with features suggestive of myelodysplastic syndrome (MDS)/acute myeloid leukaemia (AML). * Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow the formulated product or previous significant bowel resection that would preclude adequate absorption of AZD5305 * Known allergy or hypersensitivity to investigational product(s) or any of the excipients of the investigational product(s). Prior malignancy whose natural history, in the Investigator's opinion, has the potential to interfere with safety and efficacy assessments of the investigational regimen. other module-specific criteria may apply

Primary outcome measure(s)

Trial sites (68)

FacilityCityRegionStatus
Research Site Boston Massachusetts
Research Site Boston Massachusetts
Research Site New York New York
Research Site Oklahoma City Oklahoma
Research Site Houston Texas
Research Site Heidelberg Australia
Research Site Melbourne Australia
Research Site Vancouver British Columbia
Research Site Toronto Ontario
Research Site Montreal Quebec
Research Site Montreal Quebec
Research Site Beijing China
Research Site Changchun China
Research Site Changsha China
Research Site Chengdu China
Research Site Chongqing China
Research Site Guangzhou China
Research Site Harbin China
Research Site Jining China
Research Site Shandong China
Research Site Shanghai China
Research Site Shanghai China
Research Site Taiyuan China
Research Site Wuhan China
Research Site Xi'an China
Research Site Brno Czechia
Research Site Prague Czechia
Research Site Budapest Hungary
Research Site Budapest Hungary
Research Site Budapest Hungary
Research Site Milan Italy
Research Site Milan Italy
Research Site Modena Italy
Research Site Naples Italy
Research Site Padova Italy
Research Site Roma Italy
Research Site Chūōku Japan
Research Site Kōtoku Japan
Research Site Bydgoszcz Poland
Research Site Gdansk Poland

+ 28 more sites — see the full list on the official registry below.

More AstraZeneca trials in the UK

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04644068 on ClinicalTrials.gov ↗ ← All trials in the UK