Dose Finding Study of L19TNF and Doxorubicin in Patients With STS (DOXO75)

October 16, 2023 updated by: Philogen S.p.A.

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

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

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

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

Study Type

Interventional

Enrollment (Actual)

2

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • Santa Monica, California, United States, 90403
        • Sarcoma Oncology Research Center (SORC) Cancer Center of Southern California

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 83 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Sequential Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Arm L19TNF + DOXO

Patients 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 13 µg/kg i.v. will be administered on day 1, 3 and 5 of each 21-day cycle
Doxorubicin 75 mg/m2 will be administered on day 1 of each 21-day cycle

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number and type of Adverse events (AE)
Time Frame: From week 1 to week 72
Adverse event (AE) for the assessment of safety (CTCAE v. 5.0)
From week 1 to week 72
Number and type of Serious Adverse events (SAE)
Time Frame: From week 1 to week 72
Serious Adverse Events (SAE) for the assessment of safety (CTCAE v. 5.0)
From week 1 to week 72
Number and type of Drug induced liver injury (DILI)
Time Frame: From week 1 to week 72
Drug induced liver injury (DILI) assessment based on CTCAE v.5.0
From week 1 to week 72
Electrocardiogram (ECG) findings
Time Frame: From week 1 to week 72
Electrocardiogram (ECG) findings. In particular, data about QT/QTc intervals will be collected and analyzed for QT/QTc prolongation potentially caused by treatment.
From week 1 to week 72
Echocardiogram (ECHO) findings
Time Frame: From week 1 to week 72
Echocardiogram (ECHO) findings. In particular, data about QT/QTc intervals will be collected and analyzed for QT/QTc prolongation potentially caused by treatment.
From week 1 to week 72
Calculation of the body surface area (BSA)
Time Frame: From week 1 to week 72
BSA
From week 1 to week 72
Measurement of body weight
Time Frame: From week 1 to week 72
Measurement of body weight
From week 1 to week 72
Heart rate
Time Frame: From week 1 to week 72
Measurement of heart rate
From week 1 to week 72
Blood pressure
Time Frame: From week 1 to week 72
Measurement of blood pressure
From week 1 to week 72
ECOG performance status
Time Frame: From week 1 to week 72
From week 1 to week 72

Secondary Outcome Measures

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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 5, 2019

Primary Completion (Estimated)

December 1, 2023

Study Completion (Estimated)

December 1, 2023

Study Registration Dates

First Submitted

June 28, 2019

First Submitted That Met QC Criteria

July 22, 2019

First Posted (Actual)

July 25, 2019

Study Record Updates

Last Update Posted (Actual)

October 17, 2023

Last Update Submitted That Met QC Criteria

October 16, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

Yes

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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