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A Phase I Study to Evaluate the Safety and Efficacy of L19IL2 in Combination With Ruxolitinib in Patients With Advanced Solid Tumors

28 kwietnia 2026 zaktualizowane przez: Philogen S.p.A.
This trial aims to address unmet medical needs in advanced solid tumors, specifically metastatic clear cell renal carcinoma, locally advanced or metastatic pancreatic adenocarcinoma, and metastatic colorectal adenocarcinoma.

Przegląd badań

Typ studiów

Interwencyjne

Zapisy (Szacowany)

96

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

Kopia zapasowa kontaktu do badania

Lokalizacje studiów

    • Roma
      • Roma, Roma, Włochy, 00168

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

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  1. Histologically or cytologically confirmed diagnosis of one of the following tumor types for which no further approved systemic treatment options are available:

    1. Unresectable locally advanced or metastatic pancreatic ductal adenocarcinoma, that has progressed following:

      • at least one prior line containing FOLFIRINOX and/or gemcitabine plus nab-paclitaxel, and
      • at least one approved second-line regimen (e.g., 5-FU/leucovorin plus liposomal irinotecan), or where these regimens are not suitable due to contraindication or prior intolerance
    2. Metastatic proficient mismatch repair / microsatellite stable (pMMR/MSS), BRAF V600E-negative colorectal adenocarcinoma, that has progressed following:

      • at least one prior line of systemic therapy including a fluoropyrimidine and oxaliplatin or irinotecan, with or without anti-VEGF and, if RAS wild-type, with or without anti-EGFR, and
      • at least one approved subsequent line of therapy with trifluridine-tipiracil, regorafenib or fruquintinib, or where these agents are not suitable due to contraindication or prior intolerance;
    3. Metastatic clear cell renal cell carcinoma, that has progressed following:

      • at least one prior PD-(L)1-based systemic regimen, and
      • at least one VEGF-targeted tyrosine kinase inhibitor (TKI), or where these treatments are not suitable due to contraindication or prior intolerance
  2. Patients must have no further approved and available therapy options or be documented as ineligible or intolerant.
  3. Patients must have radiographic disease progression on/after the last line of prior treatment.
  4. At least one unidimensionally measurable lesion as defined by RECIST v.1.1.
  5. Eastern cooperative oncology group (ECOG) performance status ≤ 2.
  6. Patient has an estimated life expectancy of at least 12 weeks.
  7. Hemoglobin > 10.0 g/dL.
  8. Platelets ≥ 100 x 109/L.
  9. Absolute neutrophil count (ANC) ≥ 1.5 x 109/L.
  10. Negative TB test (e.g., Mantoux or Quantiferon assay).
  11. Documented negative test for HIV, HBV, HCV excluding active infection is needed. For HBV serology: the determination of HBsAg and anti-HBcAg-Ab is required. In patients with serology documenting previous exposure to HBV (i.e., anti-HBs Ab with no history of vaccination and/or anti-HBc Ab), negative serum HBV-DNA is required. For HCV: HCV-RNA or HCV antibody test. Subjects with a positive test for HCV antibody but no detection of HCV-RNA indicating no current infection are eligible.
  12. Serum creatinine < 1.5 x ULN and estimated Glomerular Filtration Rate (eGFR) value above 75 mL/min/1.73m2. An age-calibrated definition of Chronic Kidney Disease (CKD) has been proposed to distinguish age-related from disease-related changes in eGFR. For patients younger than 40 years, CKD is defined by estimated Glomerular Filtration Rate (eGFR) below 75 mL/min/1.73m2.
  13. All acute toxic effects (excluding alopecia) of any prior therapy must have been resolved to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE v.5.0) Grade ≤ 1.
  14. Women Of Childbearing Potential (WOCBP) must have negative pregnancy test results at screening. WOCBP must be using, from screening to six months following the last study treatment administration, highly effective contraception methods, as defined by the "Recommendations for contraception and pregnancy testing in clinical trials" issued by the Head of Medicine Agencies' Clinical Trial Facilitation Group and which include, for instance, progesterone-only or combined (estrogen- and progesterone-containing) hormonal contraception associated with inhibition of ovulation, intrauterine devices, intrauterine hormone-releasing systems, bilateral tubal occlusion, vasectomized partner. Double-barrier contraception is required.
  15. Male patients with WOCBP partners must agree to use simultaneously two acceptable methods of contraception (i.e. spermicidal gel plus condom) from the screening to six months following the last study treatment administration. Double-barrier contraception is required.
  16. Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests and other study procedures.

Exclusion Criteria:

  1. Patients with primary brain tumors, brain metastases or CNS disease will be excluded.
  2. Chemotherapy, immunotherapy, or radiation therapy at the tumor sites within 4 weeks prior to study treatment start.
  3. Active or history of autoimmune disease that might deteriorate when receiving an immunostimulatory agent.
  4. Previous or concurrent cancer type that is distinct from the cancer being evaluated in this study. Exception made for any other cancer curatively treated ≥ 2 years prior to study treatment start.
  5. Presence of active severe bacterial or viral infections or other severe concurrent disease, which, in the opinion of the investigator, would place the patient at undue risk or interfere with the study.
  6. Impaired cardiocirculatory functions due to any of the following conditions:

    a History within the last year of acute or subacute coronary syndromes including myocardial infarction, unstable or severe stable angina pectoris.

    b Inadequately controlled cardiac arrhythmias including atrial fibrillation. c Heart insufficiency (> Grade II, New York Heart Association (NYHA) criteria). d Any abnormalities observed during baseline ECG and Echocardiogram investigations are considered clinically significant by the investigator.

    e Uncontrolled hypertension defined by systolic blood pressure ≥ 140 mmHg and diastolic blood pressure ≥ 90 mmHg.

    f Ischemic peripheral vascular disease (Grade IIb-IV).

  7. Known arterial aneurysms.
  8. INR > 3.
  9. Inadequate liver function (ALT, AST, ALP ≥ 2.5 x ULN or total bilirubin ≥ 2.0 x ULN). At the discretion of the investigator, an increased exclusion threshold for patients with liver metastasis can be accepted as follows: ALT, AST and ALP ≥ 5 x ULN.
  10. Known uncontrolled coagulopathy or bleeding disorder, if the subject is being treated for coagulopathy or bleeding disorder and has tests within screening limits, he/she may be included.
  11. Known hepatic cirrhosis or severe pre-existing hepatic impairment (Child-Pugh class B or C).
  12. Moderate to severe respiratory failure.
  13. Patient requires or is taking systemic corticosteroids (> 10 mg/day prednisone or equivalent) or other immunosuppressant drugs on a long-term basis. Limited use of corticosteroids to treat or prevent acute hypersensitivity reactions and asthma/COPD is not considered an exclusion criterion.
  14. Known history of allergy to an excipient in study medication (e.g. IL2, ruxolitinib) or other human proteins/peptides/antibodies.
  15. Pregnancy or breast-feeding.
  16. Severe diabetic retinopathy.
  17. Recovery from major trauma including surgery within 4 weeks prior to enrollment.
  18. Patient with iatrogenic or pathologic severe immune suppression.
  19. Requirement of concurrent use of other anti-cancer treatments or agents other than study medication.
  20. Patient taking herbal medications within 7 days prior to study treatment start.
  21. Anticoagulation therapy with P2Y12 antagonists (e.g., clopidogrel, ticagrelor) and vitamin K antagonists (e.g., phenprocoumon, warfarin).

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: Nielosowe
  • Model interwencyjny: Zadanie sekwencyjne
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Experimental L19IL2 dose escalation intravenous administration
Intravenous administration
Eksperymentalny: Experimental L19IL2 + Ruxolitinib dose escalation intravenous administration
Intravenous administration
10 mg twice, oral administration
Eksperymentalny: Experimental L19IL2 + Ruxolitinib dose expansion intravenous administration
Intravenous administration
10 mg twice, oral administration

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
STEP A and STEP B: DLT
Ramy czasowe: From Day 1 to Day 28 of the treatment
Occurrence of Dose Limiting Toxicity (DLT) of L19IL2 alone and in combination with ruxolitinib
From Day 1 to Day 28 of the treatment
Safety (AE)
Ramy czasowe: Through study completion, an average of 1 year
Adverse Events (AEs) of administration of L19IL2 alone and in combination with ruxolitinib, assessed by Common Toxicity Criteria (version 5.0, CTCAE)
Through study completion, an average of 1 year
Safety (SAEs)
Ramy czasowe: Through study completion, an average of 1 year
Serious Adverse Events(SAEs) of administration of L19IL2 alone and in combination with ruxolitinib, assessed by Common Toxicity Criteria (version 5.0, CTCAE)
Through study completion, an average of 1 year
Safety (DILI)
Ramy czasowe: Through study completion, an average of 1 year
Evaluation of possible Drug Induce Liver Injury (DILI), caused by L19IL2 alone and in combination with ruxolitinib, assessed by Common Toxicity Criteria (version 5.0, CTCAE)
Through study completion, an average of 1 year

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Overall Response Rate (ORR)
Ramy czasowe: Every 8 weeks from treatment start (every 2 cycles; each cycle is 28 days)
Overall Response Rate (ORR, including CR and PR) as per RECIST 1.1
Every 8 weeks from treatment start (every 2 cycles; each cycle is 28 days)
Disease Control Rate (DCR)
Ramy czasowe: Every 8 weeks from treatment start (every 2 cycles; each cycle is 28 days)
Disease Control Rate (DCR, including CR, PR, and SD) as per RECIST 1.1
Every 8 weeks from treatment start (every 2 cycles; each cycle is 28 days)
DoR
Ramy czasowe: Every 8 weeks from treatment start (every 2 cycles; each cycle is 28 days)
Duration of Response (DoR)
Every 8 weeks from treatment start (every 2 cycles; each cycle is 28 days)
PSF
Ramy czasowe: Every 8 weeks from treatment start (every 2 cycles; each cycle is 28 days)
Progression Free Survival (PFS)
Every 8 weeks from treatment start (every 2 cycles; each cycle is 28 days)
Human anti-fusion protein antibody (HAFA)
Ramy czasowe: Day 1 and 8 of cycle 1; Day 1 of cycle 2, 3, 4, 5, 6. Each cycle is 28 days.
Blood samples will be obtained to assess the potential development of antibody to L19IL2.
Day 1 and 8 of cycle 1; Day 1 of cycle 2, 3, 4, 5, 6. Each cycle is 28 days.
Maximum Plasma Concentration (Cmax)
Ramy czasowe: Day 1, 2, 8, 15, 22, 23 of Cycle 1 and Day 1 of Cycles 2, 3, 4, 5, and 6 (each cycle is 28 days)
Maximum observed plasma concentration (Cmax) of L19IL2 and ruxolitinib following administration
Day 1, 2, 8, 15, 22, 23 of Cycle 1 and Day 1 of Cycles 2, 3, 4, 5, and 6 (each cycle is 28 days)
Time to Maximum Plasma Concentration (Tmax)
Ramy czasowe: Day 1, 2, 8, 15, 22, 23 of Cycle 1 and Day 1 of Cycles 2, 3, 4, 5, and 6 (each cycle is 28 days)
Time to reach maximum observed plasma concentration (Tmax) of L19IL2 and ruxolitinib.
Day 1, 2, 8, 15, 22, 23 of Cycle 1 and Day 1 of Cycles 2, 3, 4, 5, and 6 (each cycle is 28 days)
Area Under Concentration (AUC)
Ramy czasowe: Day 1, 2, 8, 15, 22, 23 of Cycle 1 and Day 1 of Cycles 2, 3, 4, 5, and 6 (each cycle is 28 days)
Area under the plasma concentration-time curve (AUC) of L19IL2 and ruxolitinib
Day 1, 2, 8, 15, 22, 23 of Cycle 1 and Day 1 of Cycles 2, 3, 4, 5, and 6 (each cycle is 28 days)
Terminal Elimination Half-life (t½)
Ramy czasowe: Day 1, 2, 8, 15, 22, 23 of Cycle 1 and Day 1 of Cycles 2, 3, 4, 5, and 6 (each cycle is 28 days)
Terminal elimination half-life (t½) of L19IL2 and ruxolitinib
Day 1, 2, 8, 15, 22, 23 of Cycle 1 and Day 1 of Cycles 2, 3, 4, 5, and 6 (each cycle is 28 days)

Współpracownicy i badacze

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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 maja 2026

Zakończenie podstawowe (Szacowany)

1 grudnia 2029

Ukończenie studiów (Szacowany)

1 maja 2030

Daty rejestracji na studia

Pierwszy przesłany

15 kwietnia 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

28 kwietnia 2026

Pierwszy wysłany (Rzeczywisty)

5 maja 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

5 maja 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

28 kwietnia 2026

Ostatnia weryfikacja

1 kwietnia 2026

Więcej informacji

Terminy związane z tym badaniem

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

produkt wyprodukowany i wyeksportowany z USA

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 .

Badania kliniczne na Gruczolakorak trzustki

Badania kliniczne na L19IL2

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