Clinical trial · Interventional
Pharmacokinetics, Biodistribution, Radiation Dose and Safety Study of 68Ga-NYM005 in Patients
Pharmacokinetics, Biodistribution, Radiation Dose and Safety Study of a Single Dose of Gallium [68Ga]-NYM005 Injection Prepared by Kit for the Preparation of the 68Ga-NYM005 Injection in Patients With Metastatic Clear Cell Renal Carcinoma.
NCT06389682CI-TRIAL-00089975completedPhase 1 / Phase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
68Ga-NYM005 is a CAIX-targeting small-molecular radiotracer for PET/CT imaging of clear cell renal cell carcinoma
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Clear Cell Renal Cell Carcinoma Metastatic | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 68Ga-NYM005 injection | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- 68Ga-NYM005 injection
- interventionNames
- Drug: 68Ga-NYM005 injection
Primary outcomes (1)
- measure
- Incidence of Adverse Events
- timeFrame
- 5 days
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patients with pathologically confirmed metastatic renal clear cell carcinoma; 2. Age range from 18 to 75 years old (including 18 and 75 years old); 3. ECOG score of 0 or 1; 4. Expected life \> 6 months; 5. GFR\> 60 ml/min; 6. Women of childbearing age need to have a negative pregnancy test, and the subjects(including male subjects)agree to take effective contraceptive measures during the study period and for at least three months after the drug administration; 7. The subjects are able to maintain good communication with the researchers;understand and follow the requirements of this study and sign an informed consent form before the start of relevant research operations. Exclusion Criteria: 1. Pregnant or lactating women, or women who plan to conceive during the study period or within three months after drug administration; 2. Known or suspected to be allergic to the investigational drug or any of its components,acetazolamide or other sulfonamides: 3. Accepting other investigational drugs upon enrollment, or within 5 biological half-lives of the drug at enrollment, or within 30 days after its last administration, whichever is longer; 4. Those who have used any radioactive therapy medication within 90 days before investigational drug administration, or have received any radioactive diagnostic medication within 3 days before investigational drug administration; 5. On VEGF TKI treatment less than 7 days before 68Ga-NYM005 PET/CT, such as sunitinib,sorafenib, cabozantinib, pazopanib, or lenvatinib, a washout of one week before 68Ga-NYM005 PET/CT is required; 6. Planned (for the period between injection of 68Ga-NYM005 and imaging) antineoplastic therapies; 7. Plan to arrange surgery and other invasive interventions within 2 days after the injection of the investigational drug; 8. Ongoing toxicity \>grade l from previous standard or investigational therapies; 9. Patients with active infections during screening; 10. Those who have no guarantee of being able to lie down quietly in the examination cabin during a PET examination, or those who suffer from claustrophobia and cannot cooperate in a PET examination: 11. Other situations where the researchers believe that the subject is not suitable for inclusion in this study.
References
Publications (0)
Data not yet available
No reference posted for this study.