Study of AZD5305 as Monotherapy and in Combination With Anti-cancer Agents in Patients With Advanced Solid Malignancies
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- AstraZeneca
- Study ID
- NCT04644068
- Phase
- PHASE1/PHASE2
- Status
- Active Not Recruiting
Conditions
- Additional Indications Below for Module 4 and 5
- Biliary Cancer
- Bladder Cancer
- Breast Cancer
- Cervical Cancer
- Colorectal Cancer
- Endometrial Cancer
- Gastric Cancer
- Non-small Cell Lung Cancer
- Ovarian Cancer
- Pancreatic Cancer
- Prostate Cancer
- Small Cell Lung Cancer Only in Module 5
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 130 Years
- Healthy Volunteers
- Not accepted
Interventions
- AZD5305 — DRUGOral PARP inhibitor
- Paclitaxel — DRUGIV Anti-microtubule agent
- Carboplatin — DRUGIV Platinum chemotherapeutic
- T- Dxd — DRUGIV Antibody-drug conjugate
- Dato-DXd — DRUGIV Antibody-drug conjugate
- Camizestrant — DRUGOral SERD Molecule
Study Details
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.
Key Dates
- First listed
- Nov 25, 2020
- Start date
- Nov 12, 2020
- Status verified
- Aug 2026
- Primary completion
- May 28, 2027
- Completion
- May 28, 2027
Study Design
- Enrollment
- 702 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Module 1: AZD5305 MonotherapyAZD5305 Monotherapy
- Experimental: Module 2: AZD5305 + PaclitaxelAZD5305 + Paclitaxel
- Experimental: Module 3: AZD5305 + Carboplatin with or without PaclitaxelAZD5305 + Carboplatin with or without Paclitaxel
- Experimental: Module 4: AZD5305 + Trastuzumab DeruxtecanAZD5305 + T- DXd
- Experimental: Module 5 AZD5305 + Datopotamab DeruxtecanAZD5305 + Dato-DXd
- Experimental: Module 6 AZD5305 + CamizestrantAZD5305 + Camizestrant
Primary Outcome Measure
The number of subjects with adverse events/serious adverse events [ Time Frame: From time of Informed Consent to 28 + 7 days post last dose ( modules 1,2,3,5 and 6). 40+7 days post last dose for Module 4. ]
Locations (5)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Research Site | Boston | Massachusetts | 02114 | - |
| Research Site | Boston | Massachusetts | 02215 | - |
| Research Site | New York | New York | 10021 | - |
| Research Site | Oklahoma City | Oklahoma | 73104 | - |
| Research Site | Houston | Texas | 77030 | - |
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