Testing IPN01203 for advanced solid tumor

Exclusion

• −Treatment with \>10 mg per day of prednisone (or equivalent) or other immune suppressive drugs within 7 days prior to the initiation of study drug. Exceptions may be made for participants who have had allergic reaction to iodinated contrast media. Steroids for topical, ophthalmic, inhaled, or nasal administration are allowed.
• −Have untreated or active primary brain tumour, Central Nervous System (CNS) metastases, leptomeningeal disease, or spinal cord compression.
• −Presence of hepatitis B surface antigen (HBsAg) \[or hepatitis B core antibody (HBcAb)\] at screeningScreeningThe checks done before joining, to see whether a study fits.Read more → or within 3 months prior to the first dose of study intervention.
• −Positive hepatitis C antibody test result at screening or within 3 months prior to the first dose of study intervention.
• −Participants with known history of HIV infection are excluded from the study unless they meet the following criteria:
• −Viral Load: Participants must have an undetectable viral load (HIV RNA \<50 copies/mL)
• −No Opportunistic Infections: Participants must not have had any opportunistic infections or other human immunodeficiency virus (HIV)-related illness within the past 6 months Note: HIV testing will be performed in any countries where it is mandatory per local requirements.
• −Experienced severe, life-threatening immune-mediated AEs, or infusion-related reactions such as those that lead to permanent discontinuation while on treatment with prior anticancer therapy such as immune checkpoint inhibitor therapy.
• −History of known autoimmune disease
• −History of stroke or significant cerebrovascular disease, encephalitis, meningitis, organic brain disease (e,g., Parkinson's disease) or uncontrolled seizures in the year prior to first dose of study drug.
• −Left ventricular ejection fraction \<45%
• −QT interval corrected by Fridericia (QTcF) \>470 ms (for women) and \>450 ms (for men) or CS arrhythmias.
• −History of CS respiratory disease within 6 months prior to the initiation of study intervention, including severe chronic obstructive pulmonary disease or asthma.
• −Prior organ transplantation.
• −Chronic or ongoing active infections within 4 weeks prior to Cycle1 Day1 (C1D1).
• −Stable Antiretroviral Therapy: Participants must be on a stable antiretroviral therapy regimen for at least 4 weeks prior to enrolmentEnrolmentThe number of participants a study plans to include, or has included.Read more →.
• −CD4+ T cell Count: Participants must have a CD4+ T cell count of at least 200 cells/µL.
• −History of other malignancy within the last years.
• −Significant concurrent, uncontrolled medical condition that would put participants at unacceptable risk from study participation or preclude them from complying with study procedures per investigatorPrincipal investigatorThe doctor or researcher responsible for running the study at a site.Read more → including, but not limited to renal, hepatic, haematologic, gastrointestinal, endocrine, pulmonary, neurological, cerebral, or psychiatric disease.
• −Concurrent participation in another therapeutic treatment study.
• −Participants accommodated in an institution because of regulatory or legal order; prisoners or participants who are legally institutionalised.
• −For French participants only: participants are under court protection, not affiliated to a social security system or protected adults.
• −History of CS cardiac disease within 6 months prior to the initiation of study intervention, including but not limited to unstable angina, acute myocardial infarction, endoscopic or open-heart cardiac surgery, or heart failure classified as New York Heart Association Grade 2 or higher. Additional exclusion criteriaExclusion criteriaThe things that would prevent someone from taking part.Read more → include: