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68Ga-NYM096/177Lu-NYM096 in Metastatic CcRCC

Phase 1
Recruiting
Conditions
Clear Cell Renal Cell Carcinoma
Interventions
Drug: 68Ga-NYM096 PET/CT and 177Lu-NYM096
Registration Number
NCT06649682
Lead Sponsor
Peking Union Medical College Hospital
Brief Summary

This is a single-center, phase I study. Patients with metastatic clear cell renal cell carcinoma will be recruited in this study to (Phase A) evaluate using 68Ga-NYM096 PET/CT and to (Phase B) treat with 177Lu-NYM096.

The study will be conducted in two phases. The purpose is Phase A: to evaluate the safety, tolerability, and imaging characteristics of 68Ga-NYM096 Phase B: to evaluate the safety, tolerability, and recommended phase 2 dose of 177Lu-NYM096

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
20
Inclusion Criteria
  1. Age≥18y
  2. Histologically or cytologically confirmed metastatic clear cell renal cell carcinoma
  3. Progression after or cannot undergo standard therapy with tyrosine kinase inhibitor (TKI) treatment or TKI combined with immune checkpoint inhibitor treatment.
  4. Presence of at least 1 non-irradiated tumor lesion detected at conventional imaging (computed tomography / magnetic resonance imaging (CT/MRI)) documented within 4 weeks prior to the 68Ga-NYM096 administration which should be measurable per response evaluation criteria in solid tumors (RECIST) v1.1.
  5. ECOG= 0 or 1
  6. Written informed consent.
  7. For Phase B: 68Ga-NYM096 should meet the imaging inclusion criteria
Exclusion Criteria
  1. Any major surgery within 12 weeks before enrollment
  2. Inability to stay in the scanner bed and keep still for the duration of the scan
  3. Participants who have not had resolution of clinically significant toxic effects of prior systemic cancer therapy, surgery, or radiotherapy to Grade ≤1
  4. EGFR no higher than 30ml/min*1.73m2
  5. Inflammatory bowel disease
  6. Phase A: TKI treatment within one week before 68Ga-NYM096 administration
  7. Phase B: Participants who received any systemic antineoplastic therapy for the underlying disease and/or other investigational agents within a period which is ≤5 half-lives or ≤4 weeks (whichever is shorter).
  8. Any previous CA IX-targeting treatment
  9. Prior external beam radiation therapy (EBRT) to more than 25% of the bone marrow
  10. Pregnant or breastfeeding

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Imaging and therapy68Ga-NYM096 PET/CT and 177Lu-NYM09668Ga-NYM096 PET/CT and 177Lu-NYM096
Primary Outcome Measures
NameTimeMethod
(Phase A) The number to patients with treatment-emergent adverse event (TEAE) and serious adverse event (SAE)From the start of 68Ga-NYM096 PET/CT to 1 week after the 68Ga-NYM096 PET/CT
(Phase B) The number of patients with dose-limiting toxicity (DLT) after the first treatment of 177Lu-NYM096From the start of 1st cycle of 177Lu-NYM096 treatment (each cycle is 8 weeks) to 8 weeks later.

177Lu-NYM096 will be delivered to participants up to 4 cycles with the same dosing amount. Each cycle will start 8 +/- 1 weeks after the previous cycle. The dose administrated to the participants will start at 50mCi and increase to 100, 150, and 200mCi at most in differnt dosing groups. While the AEs will be monitered for 8 months (2 months after the 4th dose), the decision whether the dose can increase to the next higher group will be decided only upon the DLT between the 1st and 2nd cycle.

Secondary Outcome Measures
NameTimeMethod
(Phase A) Dosimetry of 68Ga-NYM0961 month after the 68Ga-NYM096 PET/CT
(Phase A) Number of lesions detected by 68Ga-NYM096 PET/CT1 week after the 68Ga-NYM096 PET/CT
(Phase A) Tumor uptake of 68Ga-NYM0961 week after the 68Ga-NYM096 PET/CT
(Phase A) Optimal imaging window of 68Ga-NYM096 PET/CT1 week after the 68Ga-NYM096 PET/CT
(Phase B) The number of patients with treatment-emergent adverse event (TEAE) and serious adverse event (SAE) after 177Lu-NYM096From the start of 1st cycle of 177Lu-NYM096 administration (each cycle is 8 weeks) to 8 months later (8 weeks after the 4th cycle of treatment).

177Lu-NYM096 will be delivered to participants up to 4 cycles with the same dosing amount. Each cycle will start 8 +/- 1 weeks after the previous cycle. The administration of 177Lu-NYM096 costs about half an hour.

(Phase B) Dosimetry of 177Lu-NYM0961 month after 177Lu-NYM096 treatment
(Phase B) Radioactive concentration of 177Lu-NYM096 in the blood at different time point after 177Lu-NYM096 administrationFrom the start of 1st cycle of 177Lu-NYM096 administration (each cycle is 8 weeks) to 168 hours later.

177Lu-NYM096 will be delivered to participants up to 4 cycles with the same dosing amount. Each cycle will start 8 +/- 1 weeks after the previous cycle. The administration of 177Lu-NYM096 costs about half an hour.

(Phase B) Tumor uptake of 177Lu-NYM096 on post-therapy scan1 week after 177Lu-NYM096 administration
(Phase B) ORR (overall response rate) of 177Lu-NYM096 treatmentFrom the start of 1st cycle of 177Lu-NYM096 treatment (each cycle is 8 weeks) to 2 years later.

177Lu-NYM096 will be delivered to participants up to 4 cycles with the same dosing amount. Each cycle will start 8 +/- 1 weeks after the previous cycle. The tumor reponse will be evaluated before each cycle during the treatment (roughly every 2 months) and every 3 months after the end of the 4th cycle until 2 years after treatment start or tumor progression.

(Phase B) DCR (disease control rate) of 177Lu-NYM096 treatmentFrom the start of 1st cycle of 177Lu-NYM096 treatment (each cycle is 8 weeks) to 2 years later.

177Lu-NYM096 will be delivered to participants up to 4 cycles with the same dosing amount. Each cycle will start 8 +/- 1 weeks after the previous cycle. The tumor reponse will be evaluated before each cycle during the treatment (roughly every 2 months) and every 3 months after the end of the 4th cycle until 2 years after treatment start or tumor progression.

(Phase B) PFS (progression free survival) of 177Lu-NYM096 treatmentFrom the start of 1st cycle of 177Lu-NYM096 treatment (each cycle is 8 weeks) to 2 years later.

177Lu-NYM096 will be delivered to participants up to 4 cycles with the same dosing amount. Each cycle will start 8 +/- 1 weeks after the previous cycle. The tumor reponse will be evaluated before each cycle during the treatment (roughly every 2 months) and every 3 months after the end of the 4th cycle until 2 years after treatment start or tumor progression.

(Phase B) DOR (duration of response) of 177Lu-NYM096 treatmentFrom the start of 1st cycle of 177Lu-NYM096 treatment (each cycle is 8 weeks) to 2 years later.

177Lu-NYM096 will be delivered to participants up to 4 cycles with the same dosing amount. Each cycle will start 8 +/- 1 weeks after the previous cycle. The tumor reponse will be evaluated before each cycle during the treatment (roughly every 2 months) and every 3 months after the end of the 4th cycle until 2 years after treatment start or tumor progression.

(Phase B) OS (overall survival) of 177Lu-NYM096 treatmentFrom the start of 1st cycle of 177Lu-NYM096 treatment (each cycle is 8 weeks) to the date of first documented date of death from any cause, assessed up to 60 months.

177Lu-NYM096 will be delivered to participants up to 4 cycles with the same dosing amount. Each cycle will start 8 +/- 1 weeks after the previous cycle. The tumor reponse will be evaluated before each cycle during the treatment (roughly every 2 months) and every 3 months after the end of the 4th cycle until 2 years after treatment start or tumor progression. The survival info will be followed every 6 months until all-caused death of participant, assessed up to 60 months.

(Phase B) PFS rate at 6 months of 177Lu-NYM096 treatment6 month after the start of 1st cycle of 177Lu-NYM096 treatment (each cycle is 8 weeks) .

177Lu-NYM096 will be delivered to participants up to 4 cycles with the same dosing amount. Each cycle will start 8 +/- 1 weeks after the previous cycle. The tumor reponse will be evaluated before each cycle during the treatment (roughly every 2 months).

Trial Locations

Locations (1)

Peking Union Medical College Hospital

🇨🇳

Beijing, Beijing, China

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