Clinical Trials /

Dose Finding Study of L19TNF and Doxorubicin in Patients With STS

NCT04032964

Description:

The study is aimed at evaluating the safety of L19TNF in combination with the most appropriate dose of doxorubicin.

Related Conditions:
  • Soft Tissue Sarcoma
Recruiting Status:

Not yet recruiting

Phase:

Phase 1

Trial Eligibility

Document

Title

  • Brief Title: Dose Finding Study of L19TNF and Doxorubicin in Patients With STS
  • Official Title: A Dose Finding Study of the Tumor-targeting Human Antibody-cytokine Fusion Protein L19TNF in Combination With Doxorubicin in Patients With Advanced or Metastatic Soft Tissue Sarcoma

Clinical Trial IDs

  • ORG STUDY ID: PH-L19TNFDOX75-02/19
  • NCT ID: NCT04032964

Conditions

  • Soft Tissue Sarcoma

Interventions

DrugSynonymsArms
L19TNFArm L19TNF + DOXO
DOXORUBICINArm L19TNF + DOXO

Purpose

The study is aimed at evaluating the safety of L19TNF in combination with the most appropriate dose of doxorubicin.

Detailed Description

      Open-label, phase 1 dose confirmation study in patients with advanced, unresectable and/or
      metastatic soft tissue sarcoma.

      Six (6) Patients will be enrolled sequentially and will be treated according to the following
      scheme:

      • Doxorubicin 75 mg/m2 i.v. on day 1 of each 21-day cycle L19TNF 13 µg/kg i.v. on day 1,3 and
      5 of each 21-day cycle Initiation of the study treatment for an individual subject will occur
      no less than 3 days after initiation of the study treatment for the previous patient. Not
      more than 2 patients are to be treated simultaneously in Cycle 1.

      Should unacceptable toxicities occur in ≥ 2 patients during the observation period from Day 1
      to Day 21 (first cycle), enrollment will be stopped.

      If a patient is not evaluable for unacceptable toxicity, he/she will be replaced.

      Patients will be treated in repeated cycles until the treatment or when one of the following
      criteria are met:

        -  Unacceptable toxicity

        -  Disease Progression or relapse

        -  The patient or the investigator requests the treatment discontinuation

        -  The patient meets a withdrawal criterion. Patients with SD or PR (according to Response
           Evaluation Criteria in Solid Tumors (RECIST) v.1.1 evaluation) after the maximum of 6
           cycles of study treatment, will receive maintenance therapy for up to 18 maintenance
           cycles from start of treatment, toxicity or until disease progression occurs.
           Maintenance can start immediately after the end of cycle 6 and consists infusions of
           L19TNF on Day 1 of each maintenance cycle (every 3 weeks) and doxorubicin on Day 1 of
           maintenance cycle 1 and 2 (if appropriate).

      The primary objective is to evaluate the safety of L19TNF in combination with doxorubicin and
      to establish a recommended dose (RD), assessed as follows:

        -  Adverse events (AEs), serious adverse events (SAE) and drug induced liver injury (DILI)
           assessment based on Common Terminology Criteria for Adverse Events (CTCAE) v.5.0

        -  Standard laboratory (hematology, biochemistry and urinalysis) parameters.

        -  Electrocardiogram (ECG) and echocardiogram (ECHO) findings. In particular, data about
           QT/QTc intervals will be collected and analyzed for QT/QTc prolongation potentially
           caused by treatment.

        -  Physical examination findings including assessment of vital signs and physical
           measurements.

      The secondary objective of the study is to evaluate signs of efficacy measured as
      progression-free survival (PFS) rate at 3, 6, 9, 12 and 18 months.

      The other secondary objectives of the study are as follows:

        -  Efficacy of L19TNF in combination with doxorubicin:

        -  Overall response rate (ORR, consisting of CR and PR).

        -  Disease Control Rate (DCR, i.e. complete response (CR), partial response (PR) and stable
           disease (SD))

        -  Assessment of the formation of human anti-fusion protein antibodies (HAFA) against
           L19TNF.

        -  Characterization of pharmacokinetics (PK) of L19TNF and doxorubicin
    

Trial Arms

NameTypeDescriptionInterventions
Arm L19TNF + DOXOExperimentalPatients will be treated with: doxorubicin 75 mg/m2 i.v. on day 1 of each 21-day cycle; L19TNF 13 µg/kg i.v. on day 1, 3 and 5 of each 21-day cycle
  • L19TNF
  • DOXORUBICIN

Eligibility Criteria

        Inclusion Criteria:

          1. Age 18-85 years.

          2. Histologically confirmed diagnosis of advanced unresectable or metastatic soft tissue
             sarcoma not amenable to curative treatment with surgery or radiotherapy. Participants
             with Kaposi's sarcoma and gastrointestinal stromal tumors (GIST) will be excluded.
             Note: Evidence of disease progression is required for participants that are not newly
             diagnosed.

          3. Patients must have at least one unidimensionally measurable lesion by computed
             tomography as defined by RECIST criteria 1.1. If only one lesion is present at
             screening this lesion should not have been irradiated during previous treatments.

          4. Life expectancy of at least 3 months in the judgment of the investigator.

          5. ECOG ≤ 2.

          6. Documented negative test for HIV-HBV-HCV. For HBV serology: the determination of
             HBsAg, anti-HBsAg-Ab 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.

          7. Female patients: negative serum pregnancy test for women of childbearing potential
             (WOCBP)* within 14 days of starting treatment. WOCBP must agree to use, from the
             screening to six months following the last study drug 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 (www.hma.eu/ctfg.html) 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 or sexual abstinence. Male patients: Male subjects able to father children
             must agree to use two acceptable methods of contraception throughout the study (e.g.
             condom with spermicidal gel). Double-barrier contraception is required.

          8. Informed consent signed and dated to participate in the study.

          9. Willingness and ability to comply with the scheduled visits, treatment plan,
             laboratory tests and other study procedures.

               -  Women of childbearing potential are defined as females who have experienced
                  menarche, are not postmenopausal (12 months with no menses without an alternative
                  medical cause) and are not permanently sterilized (e.g. tubal occlusion,
                  hysterectomy, bilateral oophorectomy or bilateral salpingectomy)

        Exclusion Criteria:

          1. Diagnosis of GIST or Kaposi sarcoma.

          2. Prior therapy (except surgery and radiation) for this presentation of unresectable or
             metastatic malignant soft tissue sarcoma.

          3. Previous treatment with anthracycline- or anthracenedione-containing chemotherapy.

          4. Radiotherapy within 3 weeks (21 days) prior to therapy and previous radiation therapy
             to the mediastinal or pericardial area.

          5. Active central nervous system (CNS) or leptomeningeal metastasis (brain metastasis).
             Participants with a history of a CNS metastasis previously treated with curative
             intent (for example, stereotactic radiation or surgery) that have not progressed on
             follow-up imaging, have been asymptomatic for at least 60 days and are not receiving
             systemic corticosteroids and or/anticonvulsants, are eligible. Participants with signs
             or symptoms of neurological compromise should have appropriate radiographic imaging
             performed before randomization to rule out brain metastasis.

          6. Known history of allergy to TNF, anthracyclines, or other intravenously administered
             human proteins/peptides/antibodies.

          7. Absolute neutrophil count (ANC) < 1.5 x 109/L, platelets < 100 x 109/L and hemoglobin
             (Hb) < 9.0 g/dl.

          8. Chronically impaired renal function as expressed by creatinine clearance < 60 mL/min
             or serum creatinine > 1.5 ULN.

          9. Inadequate liver function (ALT, AST, ALP or total bilirubin ≥ 2.5 x ULN).

         10. Any severe concomitant condition which makes it undesirable for the patient to
             participate in the study or which could jeopardize compliance with the protocol.

         11. History within the last year of cerebrovascular disease and/or acute or subacute
             coronary syndromes including myocardial infarction, unstable or severe stable angina
             pectoris.

         12. Heart insufficiency (> Grade II, New York Heart Association (NYHA) criteria).

         13. Clinically significant cardiac arrhythmias or requiring permanent medication.

         14. Abnormalities observed during baseline ECG and ECHO investigations that are considered
             as clinically significant by the investigator. Subjects with current, or a history of
             QT/QTc prolongation would be excluded. In particular:

               -  patients with a marked prolongation of QT/QTc interval (e.g., repeated
                  demonstration of QTc >480 milliseconds using Fredricia's QT correction formula)
                  are excluded;

               -  patients with a history of risk factors for Torsades de Pointes (e.g., heart
                  failure, hypokalemia, family history of prolonged QT syndrome) are excluded;

               -  patients who require the use of concomitant medications that prolong the QT/QTc
                  interval are excluded.

         15. Uncontrolled hypertension.

         16. Ischemic peripheral vascular disease (Grade IIb-IV according to Leriche-Fontaine
             classification).

         17. Severe diabetic retinopathy such as severe non-proliferative retinopathy and
             proliferative retinopathy.

         18. Major trauma including major surgery (such as abdominal/cardiac/thoracic surgery)
             within 4 weeks of administration of study treatment.

         19. Pregnancy or breast-feeding.

         20. Requirement of chronic administration of corticosteroids or other immunosuppressant
             drugs. Limited use of corticosteroids to treat or prevent infusion-related reactions
             and hypersensitivity reactions is not considered an exclusion criterion.

         21. Presence of active and uncontrolled 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.

         22. Known active or latent tuberculosis (TB).

         23. Concurrent malignancies other than soft tissue sarcoma, unless the patient has been
             disease-free for at least 2 years.

         24. Growth factors or immunomodulatory agents within 7 days prior to the administration of
             study treatment.

         25. Serious, non-healing wound, ulcer or bone fracture.

         26. Allergy to study medication or excipients in study medication.

         27. Concurrent therapy with anticoagulants.

         28. Concurrent use of other anti-cancer treatments or agents other than study medication.

         29. Any recent live vaccination within 4 weeks prior to treatment or plan to receive
             vaccination during the study.
      
Maximum Eligible Age:85 Years
Minimum Eligible Age:18 Years
Eligible Gender:All
Healthy Volunteers:No

Primary Outcome Measures

Measure:Number and type of Adverse events (AE)
Time Frame:From week 1 to week 72
Safety Issue:
Description:Adverse event (AE) for the assessment of safety (CTCAE v. 5.0)

Secondary Outcome Measures

Measure:Progression-free survival (PFS) rate
Time Frame:3, 6, 9, 12 and 18 months
Safety Issue:
Description:To evaluate signs of efficacy measured as progression-free survival (PFS) rate
Measure:Efficacy of L19TNF in combination with doxorubicin: Overall response rate
Time Frame:3, 6, 9, 12 and 18 months
Safety Issue:
Description:Overall response rate (ORR, consisting of CR and PR)
Measure:Efficacy of L19TNF in combination with doxorubicin: Disease Control Rate
Time Frame:3, 6, 9, 12 and 18 months
Safety Issue:
Description:Disease Control Rate (DCR, consisting of CR, PR and SD)
Measure:HAFA measurement
Time Frame:Treatment phase: at day 1 of cycle 1, at day 8 of week 1, at day 1 of cycle 2 and at day 1 of every cycle; at day 1 of every maintenance cycle (each cycle is 21 days)
Safety Issue:
Description:Assessment of the formation of Human anti-fusion protein antibodies (HAFA) against L19TNF
Measure:PK value of L19TNF
Time Frame:Cycle 1 day 1, Cycle 1 day 2, cycle 1 day 3 and cycle 1 day 5 (each cycle is 21 days)
Safety Issue:
Description:Measurement of AUC value of L19TNF
Measure:PK value of doxorubicin
Time Frame:Cycle 1 day 1, Cycle 1 day 2, cycle 1 day 3 and cycle 1 day 5 (each cycle is 21 days)
Safety Issue:
Description:Measurement of AUC value of doxorubicin

Details

Phase:Phase 1
Primary Purpose:Interventional
Overall Status:Not yet recruiting
Lead Sponsor:Philogen S.p.A.

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