An Open-Label, Multicenter, Phase 1a/1b, Dose Escalation/Dose Expansion Clinical Trial of Theranostic Pair PD-32766D, a 64Cu-Labeled Peptide and PD-32766T, an 225Ac-Labeled Peptide Targeting Carbonic Anhydrase IX in Adult Participants With Relapsed or Refractory Clear Cell Renal Cell Carcinoma Who Have Progressed From or Could Not be Administered Due to Medical Unsuitability or Limited Access to All Standard of Care Therapies
Condition: Clear Cell Renal Cell Carcinoma
Study Type: Interventional
Clinical Trials Identifier NCT 8-digits: NCT07688187
Sponsor: PeptiDream Inc.
Phase: Phase 1
Eligibility:
- Age: minimum 18 Years maximum N/A
- Gender: All
Inclusion Criteria:
- 1. Male or female participants aged ≥18 years. 2. Participants with confirmed diagnosis of ccRCC will be included based on the following characteristics:
- Histological confirmed locally advanced, unresectable, or metastatic ccRCC, after all available standard therapy.
- Presence of evaluable disease by Response Evaluation Criteria In Solid Tumors (RECIST) guideline (defined by RECIST v1.1). 3. Presence of positive tumor uptake 4. Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 to 1. 5. The participant's with adequate organ function 6. Life expectancy of at least 12 weeks as assessed by the Investigator.
Exclusion Criteria:
- Concurrent serious (as determined by the Investigator), uncontrolled medical conditions, or life-threatening or other significant comorbid conditions.
- Any chemotherapy, radiotherapy, immunotherapy, major surgery, biologic, investigational or hormonal therapy for treatment of solid tumors within 28 days.
- Participants who have not had resolution of clinically significant toxic effects of prior systemic cancer therapy, surgery, or radiotherapy.
- Administration of a radiopharmaceutical with therapeutic intent within a period of 6 months.
- Any previous CA9 targeting treatment.
- Known hypersensitivity to the active substance or to any of the excipients of the PD-32766D and or T.
- Clinically unstable CNS tumor at the time of screening.
- History of bowel perforation or bowel infarction, history of active stomach or duodenum ulcer or fistula in the last 2 years, history of gastroesophageal reflux disease or enterocolitis Grade ≥3 according to NCI-CTCAE and/or known active gastrointestinal infection, any unresolved prior radiation-induced gastrointestinal injury.
- Acute infection requiring IV antibiotics, antivirals, or antifungals within 14 days prior to the initiation of treatment (oral treatment are allowed).
- Pregnant or breastfeeding women.
- Known active infection with human immunodeficiency virus (HIV), hepatitis C virus (HCV), or hepatitis B virus (HBV).
- Have been diagnosed with another primary malignancy.
- Have significant, uncontrolled, or active cardiovascular disease
- Bladder outflow obstruction or unmanageable urinary incontinence.
- Inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis).
- Any major surgery within 12 weeks before enrolment.
- History of psychiatric illness or social situations likely to interfere with ability to comply with protocol required assessment or give informed consent.
View trial on ClinicalTrials.gov