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.
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
- Type of treatment
- Pill or oral medicine, Injection or infusion
- 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
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.
- Conditions
- Osteosarcomas, Bone Cancer, Ewing Sarcomas
- 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 group | Role | What they receive |
|---|---|---|
| Experimental arm | Experimental | In 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.
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)
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.
- First posted1 Oct 2026
- Study startOct 2026 (estimated)
- Primary completionFeb 2031 (estimated)
- Study completionFeb 2033 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for OsteosarcomasStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- University Hospital, Strasbourg, France
- Sponsor type
- University, hospital or other
- Collaborators
- Recordati Rare Diseases Inc, Ministry of Health, France, National Cancer Institute, France
- Responsible party
- Sponsor
- Investigators
- Natacha ENTZ WERLE, MD PhD, Principal investigator, Hopitaux Universitaires de Strasbourg
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