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Phase I Study Evaluating 161Tb-PSMA Therapy in Adult Patients With Metastatic Clear Cell Renal Cell Carcinoma (PRadR2)

14 września 2026 zaktualizowane przez: Centre Leon Berard

PRadR2 - A Single Center, Open-label, Phase I Study Evaluating 161Tb-PSMA Therapy in Adult Patients With Metastatic Clear Cell Renal Cell Carcinoma

This study is an open label, Phase I study investigating the safety and clinical activity of 4 IV injections of 161Tb-PSMA-1 in patients with mccRCC.

This trial is divided in 2 parts:

  • The dose escalation part aims to assess the safety of 161Tb-PSMA-1 in up to 21 patients with mccRCC. Eligible patients will be treated with escalating activity of 161Tb-PSMA.
  • The extension part aims to collect preliminary clinical activity data of the proposed treatment.

Przegląd badań

Status

Jeszcze nie rekrutacja

Warunki

Interwencja / Leczenie

Szczegółowy opis

Patients with mccRCC will be selected, treated and followed-up as described below:

Selection step - 68Ga-PSMA PET:

A selection step at screening is mandatory for all patients in order to evaluate the PSMA expression in tumor lesions through 68Ga-PSMA PET and according to local imaging review. Only patients with PSMA expressing tumors according to eligibility criteria define din the protocol will be eligible to the treatment step.

Treatment step:

Eligible patients will be treated with escalating doses of 161Tb-PSMA-1 (from 7.4 GBq ± 10% to 11.5GBq ± 10%), intravenously (IV) for 4 cycles administered every 6 weeks. Three DL are expected to be assessed in the dose escalation part from 7.4 to 11.5 GBq ± 10%.

Dose Levels 161Tb-PSMA, IV, Q6W, 4 doses :

  • DL-1 5.5 GBq ± 10% Q6W
  • DL1 (starting activity) 7.4 GBq ± 10% Q6W
  • DL2 9.5 GBq ± 10% Q6W
  • DL3 11.5 GBq ± 10% Q6W

Assessment step:

To assess tumor response according to RECIST V1.1, imaging will be performed at baseline, W9-10, W24, then every 12 weeks up to 1 year after the first administration and every 24 weeks afterwards until progression, death or overall study completion, whichever is earliest. Survival status will be documented for all patients until death or overall study completion at least 12 months after the last patient. Moreover, to study the distribution of the 161Tb-PSMA-1 in standard organs and tumor lesions, repeated SPECT-CT acquisitions will be performed on all patients treated in the dose escalation part.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

26

Faza

  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dziecko
  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  • I1. Male or female patients aged ≥ 18 years at time of informed consent signature.
  • I2. Patient with histologically confirmed diagnosis of metastatic clear cell renal cell carcinoma (mccRCC) progressing during or after at least 2 lines of therapy including at least 1 line of anti-VEGFR and 1 line of immunotherapy.
  • I3. Patient with documented radiological disease progression at the time of inclusion with measurable disease as per RECIST v1.1.
  • I4. Patient with positive PSMA-PET (68Ga-PSMA-PET) (see Appendix 6):

    • For patient with only extrahepatic disease: ≥ 50% of positive extrahepatic lesions
    • For patient with both extra-hepatic and liver metastasis: ≥ 50% of positive extrahepatic metastatic lesions and ≥ 80 % of positive supracentimetric liver metastatic lesions.
    • For patient with only liver metastatic lesions: ≥ 80 % of positive supracentimetric lesions
  • I5. Life expectancy ≥ 6 months.
  • I6. Eastern Cooperative Oncology Group performance status (ECOG PS) 0-1, with a Karnofsky Performance Status (KPS) ≥ 80%.
  • I7. Adequate organ function according to laboratory values defined below:

Haematological function :

  • Peripheral absolute neutrophil count (ANC) ≥1.5 x 109 /L
  • Platelet count ≥ 100 x 109/L
  • Hemoglobin ≥ 9.0 g/dL (without transfusion within 7 days)

Renal and hepatic function :

  • Serum creatinine or creatinine clearance according to CKD-EPI

    o ≤ 1.5 X upper limit of normal (ULN) OR ≥ 40 mL/min/1.73m2

  • Total bilirubin

    o ≤ 1.5 X ULN with the following exception: Patients with known Gilbert disease who have serum bilirubin level ≤ 3 x ULN may be enrolled

  • Aspartate aminotransferase (ASAT) and Alanine aminotransferase (ALAT) ≤ 1.5 X ULN (up to 3x ULN in case of liver metastases)

    • I8. Women of child-bearing potential must have a negative pregnancy test at screening (within 72 hours prior C1D1) and must agree to use 1 highly effective form of contraception from the time of the treatment period and of the negative pregnancy test up to 6 months after the last administration of IMP. Effective forms of contraception are listed in Appendix 5.
    • I9. Fertile males must use a highly effective contraception during dosing period and through 6 months after final administration of study.
    • I10. Patient should be able and willing to comply with study visits and procedures as per protocol.
    • I11. Patient should understand, sign, and date the written voluntary informed consent form at the screening visit prior to any protocol-specific procedures performed.
    • I12. Covered by a medical insurance.

Exclusion Criteria:

  • E1. Patients with known active central nervous system (CNS) metastases and/or epidural metastases and/or leptomeningitis. Patients with previously treated brain metastases may participate provided they are stable (without evidence of progression by imaging for at least four weeks prior to C1D1 and any neurologic symptoms have returned to baseline), have no evidence of new or enlarging brain metastases, and are not using steroids (at doses higher than 10 mg/d of methylprednisolone or equivalent) for at least 4 weeks prior to C1D1.
  • E2. Patients previously treated with any radiopharmaceutical.
  • E3. Persisting AEs related to previous anti-cancer therapy which were not resolved to grade ≤ 1 (except: anemia provided that criterion I7 is met) and /or any persistent immune-related AEs >1 (except adequately controlled irAE, e.g.: with replacement therapy for endocrine irAE) using NCI CTCAE V6.0.
  • E4. History, within 2 years, of cancer other than renal cancer, except for basal or squamous cell carcinoma of the skin, in situ carcinoma of the cervix or localized prostate cancer.
  • E5. History of idiopathic pulmonary fibrosis, non-infectious pneumonitis, interstitial lung disease that required steroids or has current pneumonitis, interstitial lung disease, drug-induced pneumonitis, or evidence of active pneumonitis.
  • E6. Prior therapy or needs to be treated with a forbidden concomitant/concurrent therapies/procedures including (see protocol for minimal wash out period to C1D1 and use during treatment) :
  • Any anticancer treatment (immunotherapy, chemotherapy) or investigational therapy
  • Targeted therapy including antiangiogenic therapy
  • Radiotherapy
  • Major surgery
  • Growth factors targeting the myeloid lineage (e.g., G-CSF, GM-CSF, M-CSF) or growth factors targeting the erythroid lineage (e.g., erythropoietin)
  • Live or live-attenuated vaccine. Note: killed vaccines are allowed.
  • E7. Patients with clinically significant hematuria, hematemesis or hemoptysis exceeding 0.5 teaspoon (2.5mL) of red blood, as well as those with a history of coagulopathy or other significant bleeding (e.g., pulmonary hemorrhage) within the 3 months prior to the initiation of the study treatment. Patients receiving anticoagulation medication will be eligible only if the dosage and route of administration have remained stable for at least 2 weeks prior to C1D1.
  • E8. Patients with an active uncontrolled infection.
  • E9. Pregnant or breastfeeding women.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: 161Tb-PSMA-1
Radiopharmaceutical - injectable solution

161Tb-PSMA-1 (from 7.4 GBq ± 10% to 11.5GBq ± 10%), intravenously (IV) for 4 cycles administered every 6 weeks.

Dose Levels 161Tb-PSMA, IV, Q6W, 4 doses

  • DL-1 5.5 GBq ± 10% Q6W
  • DL1 (starting activity) 7.4 GBq ± 10% Q6W
  • DL2 9.5 GBq ± 10% Q6W
  • DL3 11.5 GBq ± 10% Q6W

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Ramy czasowe
Incidence of Dose-limiting toxicities (DLT)
Ramy czasowe: During the first cycle of treatment (i.e., first 6 weeks)
During the first cycle of treatment (i.e., first 6 weeks)

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Objective Response Rate at 24 weeks (ORR-24W)
Ramy czasowe: 24 weeks after treatment start
24 weeks after treatment start
Objective Response Rate (ORR)
Ramy czasowe: Assessed through study completion, an average of 12 months.
defined as the rate of patients with a complete or partial response (CR or PR) according to RECIST v1.1.
Assessed through study completion, an average of 12 months.
Disease Control Rate after 24 weeks (DCR24w)
Ramy czasowe: 24 weeks after treatment start
24 weeks after treatment start
Best Overall Response Rate (BORR)
Ramy czasowe: Assessed through study completion, an average of 12 months.
Assessed through study completion, an average of 12 months.
Duration of response (DOR)
Ramy czasowe: From the date of first documented response until date of documented progression per RECIST 1.1 or death due to any cause, assessed through study completion, an average of 12 months.
From the date of first documented response until date of documented progression per RECIST 1.1 or death due to any cause, assessed through study completion, an average of 12 months.
Progression Free Survival (PFS)
Ramy czasowe: From treatment start until the date of documented progression or death due to any cause, assessed through study completion, an average of 12 months.
From treatment start until the date of documented progression or death due to any cause, assessed through study completion, an average of 12 months.
Overall Survival (OS)
Ramy czasowe: From treatment start to the date of death, assessed through study completion, an average of 12 months.
From treatment start to the date of death, assessed through study completion, an average of 12 months.

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

1 listopada 2026

Zakończenie podstawowe (Szacowany)

1 listopada 2028

Ukończenie studiów (Szacowany)

1 listopada 2029

Daty rejestracji na studia

Pierwszy przesłany

3 września 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

14 września 2026

Pierwszy wysłany (Rzeczywisty)

18 września 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

18 września 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

14 września 2026

Ostatnia weryfikacja

1 września 2026

Więcej informacji

Terminy związane z tym badaniem

Słowa kluczowe

Inne numery identyfikacyjne badania

  • ET26-035
  • 2026-525526-38-00 (Ctis)

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .