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OsteosarcomasPhase 1/2BONE DINIRRANCT07853105

Phase I/II Trial of Dinutuximab Beta in Combination With Irinotecan and Rapamycin in Pediatric, Adolescents and Adult Patients With Relapsed/Refractory Bone Tumors.

A Phase 1/2 study testing Dinutuximab beta, Sirolimus and Irinotecan in people with Osteosarcomas and Bone Cancer, run by University Hospital, Strasbourg, France at 12 sites in France.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

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Trial summary

Osteosarcomas, like other primitive bone tumors, remain hard-to-treat malignancies, especially after failure of first-line treatments. Multiple mechanisms are initiating or rendering bone tumor cells resistant to the chemotherapies leading to the drastic reduction of treatment possibilities in case of relapses. Read more about this study

Who is it for?
Ages 6 to 40 years
Conditions the study is for
Osteosarcomas, Bone Cancer, Ewing Sarcomas
What is being tested?
Dinutuximab beta, Sirolimus and Irinotecan
Could I receive a placebo?
No, everyone receives an active treatment
How many people
89 participants
Where
12 sitesFrance
Study dates
Oct 2026to Feb 2033
Phase
Phase 1/2

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 40 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • Biopsy proven osteosarcomas, Ewing sarcomas, other primitive bone cancers (chondrosarcomas, CIC-DUX4 bone sarcomas, Ewing-like tumors with rare fusions). Patients with relapsed refractory tumors are eligible whether the target tumor(s) is(are) considered resectable or unresectable at study entry, provided that immediate surgery is not considered medically required or immediately feasible. For tumors considered potentially resectable, resectability will be reassessed after study treatment, particularly at week 16, within a multidisciplinary tumor board.
  • Refractory or relapsed sarcomas with no brain metastasis.
  • 1 to 3 prior treatments for metastatic or locally advanced sarcoma.
  • Age ≥ 6 and ≤ 40 years at inclusion.
  • Performance status: Lansky Play score (for patients ≤ 16 years of age) or Karnofsky score (for patients > 16 years of age) ≥ 70%.
  • Life expectancy expected ≥ 4 months.
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  • - For Phase I exclusively, patients must have radiographically documented evaluable or measurable progressive disease by CT-scan, IRM or PET-scan 18F-FDG (measure of SUL and extension).
  • For Phase II exclusively, patients must have radiographically documented measurable and evaluable progressive disease. At least one site of disease might be measurable as follows: i. CT-scan, physical exam ≥10 mm ii. Chest X-ray ≥20 mm iii. Lymph node short axis ≥10 mm iv. Bone and marrow invasion on PET-scan FDG (measure of SUL and extension) All radiology studies must be performed between 7 and 28 days before the first dose of study treatment (C1D1).
  • Adequate cardiac function with a shortening fraction ≥29% and left ventricular ejection fraction ≥50% at baseline (between 7 and 28 days before the first dose of study treatment (C1D1)), as determined by echocardiography.
  • Adequate organ function within 21 days prior to first dose of study treatment:
  • Hematologic criteria:
  • Peripheral absolute neutrophil count (ANC) ≥1.0 × 109/L (unsupported),
  • Absolute granulocytes ≥1.0 × 109/L,
  • Platelets ≥100 × 109/L (unsupported),
  • INR (International normalized ratio) ≤1.5 and aPTT (activated partial thromboplastin time) within normal limits.
  • Biochemistry:
  • Serum creatinine ≤1.5 x upper limit of normal (ULN) for age or creatinine clearance (CKD-EPI/Schwartz) ≥ 60 mL/min/1.73 m2,
  • Total bilirubin ≤1.5 x ULN (≤3.0 x ULN for patients with Gilbert's syndrome),
  • Alanine aminotransferase (ALT)/Serum glutamic pyruvic transaminase (SGPT) ≤2.5 × ULN and Aspartate aminotransferase (AST)/Serum glutamic oxaloacetic transaminase (SGOT) ≤2.5 × ULN, except in patients with documented tumor involvement of the liver who must have ALT/SGPT and AST/SGOT ≤5 x ULN.
  • Females of childbearing potential (WOCBP) must have a negative serum pregnancy test within 72 hours prior to first dose of study treatment.
  • Sexually active WOCBP must agree to use a highly effective contraception method during the study treatment and for at least 6 months after the last study treatment administration.
  • -Sexually active male patients must agree to use condoms during the study and at least 3 months after the last study treatment administration. Acceptable contraception methods are listed in X.1 Contraception.
  • Written informed consent from parents/legal representative, patient, and age-appropriate assent before any study-specific screening procedures are conducted, according to local, regional or national guidelines.
  • Patients able to comply with study procedures, scheduled follow-up and with management of toxicity.
  • Patient affiliated to a social security regimen or beneficiary of the same according to local requirement

Who cannot join

  • Absence of tumor target(s): for Phase I: absence of visible and evaluable target; for Phase II: absence of evaluable target.
  • Prior administration of mTOR inhibitors.
  • Impairment of gastrointestinal (GI) function or GI disease that may significantly alter drug absorption of oral drugs (e.g., chronic inflammatory bowel disease, ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, or malabsorption syndrome).
  • Clinically significant uncontrolled heart disease (including history of any cardiac arrhythmias, e.g., ventricular, supraventricular, nodal arrhythmias, or conduction abnormality), congestive heart failure > class II NYHA with 12 months of screening, unstable angina or new-onset angina.
  • Prior medical history of uncontrolled hypertension defined as follow:
  • Patients aged ≤ 17 years: greater than 95th percentile systolic and diastolic blood pressure based on age and weight which is not controlled by one anti-hypertensive medication.
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  • Patients aged > 17 years: systolic blood pressure > 150mmHg and/or diastolic > 90 mmHg that is not controlled by one anti-hypertensive medication.
  • Thrombotic or embolic events within the past 6 months.
  • Evidence of interstitial lung disease.
  • Non-controlled hyperlipidemia: At fasting: Serum cholesterol >3 g/L or 7.75mmol/L and Triglycerides >2.5 ULN).
  • Constitutional abnormality of coagulation and/or hemostasis.
  • Type I diabetes or non-controlled diabetes (fasting glycemia >1.5 ULN).
  • Active viral hepatitis (serologically Hepatitis B virus (HBV) and/or Hepatitis C virus (HCV)) or known human immunodeficiency virus (HIV) infection or any other uncontrolled active clinically serious infection of grade ≥2 defined by CTCAE v6.0.
  • Serious non-healing wound, ulcer, or bone fracture at enrolment.
  • Presence of any persistent grade ≥2 treatment-related toxicity with the exception of lymphopenia of any grade, alopecia, ototoxicity or peripheral neuropathy.
  • Systemic anticancer therapy within 21 days of the first study dose or 5 times its half-life, whichever is less.
  • Previous myeloablative therapy with autologous hematopoietic stem cell rescue within 8 weeks of the first dose of study treatment.
  • Radiotherapy (non-palliative) within 21 days prior to the first study dose.
  • Major surgery or significant traumatic injury within 21 days of the first study dose. Gastrostomy, ventriculo-peritoneal shunt, endoscopic ventriculostomy, tumor biopsy and insertion of central venous access devices are not considered major surgery, but for these procedures, a 48-hour interval must be maintained before the first dose of the investigational drug is administered.
  • History of another malignancy or any medical condition which in the opinion of the principal investigator could represent a risk for the patient or adversely affect the study objectives.
  • Current therapeutic anticoagulation with Vitamin K antagonists.
  • Concomitant treatment with medications or substances that are inhibitors or inducers of cytochrome CYP450 3A4.
  • Concomitant treatment with corticosteroids within 14 days prior to the first dose of study treatment.
  • Known hypersensitivity to any study drugs or components of the formulation.
  • Pregnant or nursing lactating females.
  • Vaccinated with live, attenuated vaccines, within 4 weeks of the first dose of study drug.
  • Participation in other interventional clinical trials.
  • Patient who has difficulty reading or understanding French
  • Patient receiving government medical aid (Aide Médicale d'Etat - AME).
  • Incompetent participant (subject to a legal protection measure: curatorship, guardianship, future protection mandate, family habilitation).

Trial locations and contacts

12 sites in 1 country. Contact the study team or a site near you to ask about taking part.

12 sites in 1 country

France12 sites
  • Oncologie Médicale-Institut Bergonié

    Bordeaux

    Maud TOULMONDE, MD, 05 56 33 32 30 ext. +33, m.toulmonde@bordeaux.unicancer.fr

    Maud TOULMONDE

  • Unité d'Hémato-Oncologie Pédiatrique (UHOP) -CHU de Bordeaux - GH Pellegrin

    Bordeaux

    Jordane CHAIX, 05 57 82 04 32 ext. +33, jordane.chaix@chu-bordeaux.fr

    Jordane CHAIX

  • Oncologie - Unité pédiatrique Centre Oscar Lambret

    Lille, 59000

    Cyril LERVAT, MD, 03 20 29 59 35 ext. +33, c-lervat@o-lambret.fr

    Cyril LERVAT

  • Institut d'hématologie et d'oncologie Pédiatrique iHOPE

    Lyon

    Nadège CORRADINI, 04 69 16 26 42 ext. +33, nadege.corradini@ihope.fr

    Nadège CORRADINI

  • Oncologie médicale adulte- Centre Léon Bérard

    Lyon

    Mehdi BRAHMI, 04 78 78 27 57 ext. +33, Mehdi.BRAHMI@lyon.unicancer.fr

    Mehdi BRAHMI

  • Hématologie, Immunologie et Oncologie Pédiatrique (HIOP), CHU Timone Enfants,

    Marseille

    Gabriel REVON RIVIERE, 04 91 38 68 21 ext. +33, Gabriel.REVON-RIVIERE@ap-hm.fr

    Gabriel REVON RIVIERE

  • Onco-hématologie pédiatrique- CHRU NANCY-BRABOIS

    Nancy

    Ludovic MANSUY, MD, 03-83-15-48-74 ext. +33, lu.mansuy@chru-nancy.fr

    Ludovic MANSUY

  • Oncologie Médicale - Institut Curie

    Paris

    Valérie LAURENCE, MD, 01 44 32 46 65 ext. +33, valerie.laurence@curie.fr

    Valérie LAURENCE

  • Oncopédiatrie-SIREDO - Institut Curie

    Paris

    Sarah WINTER, MD, sarah.winter@curie.fr

    Sarah WINTER

  • Oncologie médicale, Hôpitaux Universitaires de Strasbourg

    Strasbourg, 67000

    Justine GANTZER, MD, 03 68 76 72 25 ext. +33, justine.gantzer@chru-strasbourg.fr

    Justine GANTZER

  • Onco-hématologie pédiatrique- Hôpitaux Universitaires de Strasbourg

    Strasbourg, 67098

    Natacha ENTZ WERLE, MD, PhD, 03 88 12 83 89 ext. +33, natacha.entz-werle@chru-strasbourg.fr

    Natacha ENTZ WERLE, MD, PhD

  • Unité d'Hématologie Immunologie Oncologie Pédiatrique, CHU Toulouse

    Toulouse

    Marie-Pierre CASTEX, MD, 05 34 55 86 10 ext. +33, castex.mp@chu-toulouse.fr

    Marie-Pierre CASTEX

Other trials in France

About this study

Osteosarcomas, like other primitive bone tumors, remain hard-to-treat malignancies, especially after failure of first-line treatments. Multiple mechanisms are initiating or rendering bone tumor cells resistant to the chemotherapies leading to the drastic reduction of treatment possibilities in case of relapses. Among the list of extra-tumoral mechanisms enabling this cancer cell resistance, hypoxia and tumor-associated macrophage modulation seem to be in the top ranks. Based on that, we generated by the past tumor data where the study of hypoxic biomarkers' expressions and the presence of protumoral macrophages were influencing the prognosis of osteosarcoma patients. In fact, the association of HIF1 hyperexpression and a high number of M2 phenotype macrophages (e.g., protumoral cells) were predictive markers of the worst outcome. We recently redone this translational approach in other bone tumors like Ewing sarcomas (EWS) showing the same prognostic tendency. Furthermore, a past pediatric phase I trial, named RAPIRI, targeting both mTor and HIF1, with combination of Sirolimus and Irinotecan, was able to provide in the relapsing bone cancers a partial response or stable disease in more than 50% of patients and particularly in patients with blood concentrations of Sirolimus between 5 and 15 µg/L. To go further and understand the potential links between macrophages and hypoxic resistant tumors, recent preliminary exploration, with an immunofluorescent assessment targeting GD2 expression on tumor cell membranes, was underlining osteosarcomas but also EWS with standard fusions and CIC-DUX4 cancers as hyperexpressing cancers for this disialoganglioside. The cell-surface molecule was highly expressed in 22 out of 32 diagnostic samples (unpublished data). This glycosphingolipid usually presenting a restricted pattern of expression on normal tissues seems to be frequently hyperexpressed in some cancers and therefore amenable to targeting by the monoclonal antibody Dinutuximab beta. The anti-GD2 effect of this drug relies on complement and immune effector cells to mediate cancer cell killing. Recent and unpublished preclinical data in our Lab (UMR-CNRS7021, Strasbourg) envisioned the proof-of-concept combining Sirolimus, Irinotecan and Dinutuximab beta in osteosarcoma models and afford sustainable results to conclude to a clear efficiency of this triple combination stopping completely osteosarcoma cell proliferation and reducing drastically their invasion in microenvironment. Gathering all those prerequisite data and, as the monoclonal therapeutic antibody (Dinutuximab beta) now is extensively evaluated in clinics in multiple indications (e.g., neuroblastomas, Ewing sarcomas and other sarcomas), we propose here a phase I/II trial with this combination of treatments targeting hypoxia and GD2 in bone tumors focusing on relapsing bone tumors with endpoints determining accurate dose to give to patients and its efficacy at 16 weeks of treatment.

Being tested
Dinutuximab beta, Sirolimus and Irinotecan
Keywords
anti GD2, dinutuximab beta
Medical subject headings
Osteosarcoma, Bone Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Dinutuximab beta, Sirolimus and IrinotecanDrug

    The dose escalation (Phase I) part will determine the maximum tolerated dose (MTD) of Dinutuximab beta in combination with fixed doses of Sirolimus and Irinotecan (RAPIRI), as follows: iv. irinotecan on days 1 and 15 (125 mg/m2/dose) and oral Sirolimus given daily (1.5 mg/m2/dose) in 28-day courses. The Dinutuximab beta will be administered for 4 days from D1 to D4 and D15 to D18 as an iv. infusion. The combination of Sirolimus and Irinotecan plus Dinutuximab beta will be during the 6 first courses and from C7, the Sirolimus and Irinotecan combination will be administered as detailed above during the last 6 months or courses.

    For the Phase II part, the RP2D dose of Dinutuximab beta will be used in combination with the fixed dose of Sirolimus and Irinotecan combination as described above. The same scheme during the 12 months will be planned: triple combination during 6 courses and then a maintenance with 6 courses of Sirolimus and Irinotecan treatment.

Study groups in NCT07853105
Study groupRoleWhat they receive
Experimental armExperimentalIn Phase I, the dose escalation part will determine the maximum tolerated dose (MTD) of Dinutuximab beta in combination with fixed doses of Sirolimus and Irinotecan. For the Phase II part, the RP2D (recommended phase 2 dose) dose of Dinutuximab beta will be used in combination with the fixed dose of Sirolimus and Irinotecan combination.
Receives: Drug: Dinutuximab beta, Sirolimus and Irinotecan

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Phase 1: Determination of the maximum tolerated dose (MTD) of Dinutuximab beta, given in combination with iv. Irinotecan (day 1 and day 15) and daily oral Sirolimus

    Measured: From the first dose of treatment to the end of cycle 1 (28 days)

  2. Phase 2:

    Determination of the Progression Free Survival rate, based on investigator assessment per Response Evaluation Criteria In Solid Tumors (RECIST 1.1) version 1.1 and/or PET Response Criteria In Solid Tumor version 1.0 (PERCIST 1.0).

    Measured: At or before 16 weeks after the first dose of study drug

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Oct 2026
  2. Study startOct 2026 (estimated)
  3. Primary completionFeb 2031 (estimated)
  4. Study completionFeb 2033 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1/2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
89 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07853105
Sponsor's protocol ID
9422
Acronym
BONE DINIRRA
Status last verified
Aug 2026
First submitted
31 Aug 2026
Last updated
1 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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