A Phase I/IIa Study of AZD8205 Given Alone or in Combination With Anticancer Drugs, in Participants With Advanced or Metastatic Solid Malignancies

Key Inclusion Criteria:

• Age ≥ 18 years

• Relapsed/metastatic solid tumors treated with prior adequate standard of caretherapy for tumor type and stage of disease or where in the opinion of theInvestigator, a clinical trial is the best option for the next treatment based onresponse and/or tolerability to prior therapy.

• Measurable disease per RECIST v1.1

• Eastern Cooperative Oncology Group (ECOG) Performance Status: 0-1

• Life expectancy ≥ 12 weeks

• Adequate bone marrow, hepatic, and renal function as defined in the protocol

Additional Inclusion Criteria For Sub-Study 1 Part A:

• Histologically or cytologically confirmed metastatic or locally advanced/recurrent breast cancer, ovarian cancer, BTC or endometrial cancer

Additional Inclusion Criteria For Sub-Study 1 Part B:

• Histologically or cytologically confirmed metastatic or locally advanced andrecurrent disease for the respective cohort:

1. Cohort B1 (Biliary Tract Cancer)

2. Cohort B2 (Ovarian Cancer)

3. Cohort B3 (Breast Cancer)

4. Cohort B4 (Endometrial Cancer)

5. Cohort B5 (Squamous Non-Small Cell Lung Cancer)Additional Inclusion Criteria For Sub-Study 2 Part A:

• Minimum body weight ≥ 30 kg.

• Histologically or cytologically confirmed metastatic or locally advanced/recurrentbreast cancer, ovarian cancer, BTC, endometrial cancer or squamous non-small celllung cancer.

Additional Inclusion Criteria For Sub-Study 3 Part A:

• Minimum body weight ≥ 30 kg (for participants enrolled in cohorts includingrilvegostomig only).

• Histologically or cytologically confirmed metastatic or locally advanced/recurrentbreast cancer, ovarian cancer, BTC, endometrial cancer or squamous non-small celllung cancer.

Key Exclusion Criteria:

• Treatment with any of the following:

1. Nitrosourea or mitomycin C within 6 weeks prior to the first dose of studytreatment

2. Any investigational agents or study drugs from a previous clinical study within 5 half-lives or 28 days (whichever is shorter) prior to the first dose of studytreatment

3. Any other anticancer treatment within the following time periods prior to thefirst dose of study intervention:

4. Cytotoxic treatment: 21 days

5. Non-cytotoxic drugs: 21 days or 5 half-lives (whichever is shorter)

6. Biological products including immuno-oncology agents: 28 days

• Spinal cord compression or a history of leptomeningeal carcinomatosis.

• Brain metastases unless treated, asymptomatic, stable, and not requiring continuouscorticosteroids at a dose of > 10 mg prednisone/day or equivalent for at least 4weeks prior to start of study.

• Active infection including tuberculosis and HBV, HCV or HIV

• History of (non-infectious) ILD/pneumonitis that required steroids, has currentILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imagingat screening.

• Clinically severe pulmonary compromise resulting from intercurrent pulmonaryillnesses

• Participants with any of the following cardiac criteria:

1. History of arrhythmia which is symptomatic or requires treatment (NCI CTCAEv5.0 Grade 3); symptomatic or uncontrolled atrial fibrillation, or asymptomaticsustained ventricular tachycardia.

2. Uncontrolled hypertension.

3. Acute coronary syndrome/acute myocardial infarction, unstable angina pectoris,coronary intervention procedure with percutaneous coronary intervention, orcoronary artery bypass grafting within 6 months.

4. History of brain perfusion problems (eg, carotid stenosis) or stroke, ortransient ischemic attack in the last 6 months prior to screening.

5. Symptomatic heart failure (NYHA class ≥ 2).

6. Prior or current cardiomyopathy.

7. Severe valvular heart disease.

8. Mean resting QTcF > 470 msec.

9. Risk factors for QTc prolongation or risk of arrhythmic events such as heartfailure, congenital long QT syndrome, family history of long QT syndrome orunexplained sudden death under 40 years of age.

Additional Exclusion Criteria For Sub-Study 2 Part A:

• Thromboembolic event within 3 months before the first dose of study intervention -No longer applicable per amendment 7

• Experienced a toxicity that led to permanent discontinuation of prior immunotherapy.

• Active or prior documented autoimmune or inflammatory disorders requiring chronictreatment with steroids or other immunosuppressive treatment.

• History of organ transplant

Additional Exclusion Criteria For Sub-Study 3 Part A:

• Concomitant use of medications or herbal supplements known to be strong cytochrome P (CYP) 3A4 inducers/inhibitors.

• Any history of persisting (> 2 weeks) severe cytopenia due to any cause

• Patients with any known predisposition to bleeding

• Patients with history of myelodysplastic syndrome (MDS)/acute myeloid leukemia (AML)or with features suggestive of MDS/AML (as determined by prior diagnosticinvestigation).

• Refractory nausea and vomiting, chronic gastrointestinal diseases, inability toswallow the formulated product or previous significant bowel resection that wouldpreclude adequate absorption of saruparib.