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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 aprile 2026 aggiornato da: 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.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

96

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Roma
      • Roma, Roma, Italia, 00168
        • Fondazione Policlinico Gemelli Unità di Fase 1: Unità di Farmacologia Clinica
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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).

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Non randomizzato
  • Modello interventistico: Assegnazione sequenziale
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Experimental L19IL2 dose escalation intravenous administration
Intravenous administration
Sperimentale: Experimental L19IL2 + Ruxolitinib dose escalation intravenous administration
Intravenous administration
10 mg twice, oral administration
Sperimentale: Experimental L19IL2 + Ruxolitinib dose expansion intravenous administration
Intravenous administration
10 mg twice, oral administration

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
STEP A and STEP B: DLT
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Overall Response Rate (ORR)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 maggio 2026

Completamento primario (Stimato)

1 dicembre 2029

Completamento dello studio (Stimato)

1 maggio 2030

Date di iscrizione allo studio

Primo inviato

15 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

28 aprile 2026

Primo Inserito (Effettivo)

5 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

5 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

28 aprile 2026

Ultimo verificato

1 aprile 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su L19IL2

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