Clinical trial locations
Study on the Safety and Tumor-Fighting Effects of OMO-103 for Patients with Advanced Osteosarcoma
This trial, conducted in Spain, is evaluating a new medication called OMO-103 (also known as Omomyc) for patients with advanced high-grade osteosarcoma. The treatment is delivered directly into the bloodstream through intravenous infusion.
Who can participate: Patients aged 12 years or older with confirmed advanced high-grade osteosarcoma that cannot be treated with local therapies. The disease must have progressed after at least one, but no more than two, previous chemotherapy treatments containing cisplatin and anthracycline. The cancer must be measurable using imaging tests like CT or MRI scans. Patients over 16 years old need to provide a fresh tumor sample. Both male and female participants must agree to use effective birth control starting at least one menstrual cycle before treatment and continuing for three months after the last dose.
Who cannot participate: Patients with other types of cancer besides high-grade osteosarcoma, those outside the specified age range, vulnerable populations requiring special protection, and anyone unable to follow study procedures or take the medication as required are excluded.
Study focus: The main goal is to evaluate the safety of OMO-103 and measure progression-free survival at 16 weeks. The study will monitor tumor response using imaging techniques, assess side effects through routine tests and physical examinations, and evaluate the impact on patients' quality of life using specific questionnaires. OMO-103 works by inhibiting the Myc protein, which plays a role in cancer cell growth and survival.
Study on the Effectiveness and Safety of Regorafenib for Patients with Resistant Primary Bone Tumors
This Polish trial is studying regorafenib for patients with refractory primary bone tumors, including Ewing's sarcoma and osteosarcoma, that have not responded to previous treatments. The medication is taken orally as a film-coated tablet.
Who can participate: Patients between 9 and 21 years old with Ewing's sarcoma or osteosarcoma confirmed by tissue examination. The cancer must have not responded to previous treatments or have returned, identified no earlier than 30 days before starting the study. Patients must have a life expectancy of at least 12 weeks, be able to swallow tablets, and if in puberty, must agree to use effective birth control during treatment and for at least 2 years afterward.
Who cannot participate: Patients without refractory primary bone tumors, those outside the specified age range, pregnant or breastfeeding patients, those participating in another clinical trial, and those with allergies to the study medication are excluded.
Study focus: The trial aims to determine if regorafenib can help control the disease and improve quality of life. The dosage is adjusted to achieve drug exposure similar to that recommended for adults, especially for patients aged 9 to 18 years. Regular assessments include monitoring vital signs, laboratory tests, echocardiography, and ECG to evaluate safety. The study is estimated to conclude by December 31, 2025.
Summary
These four clinical trials represent important research efforts to find more effective treatments for metastatic osteosarcoma and related bone sarcomas. The studies are geographically diverse, taking place in Spain, Italy, France, and Poland, providing access to patients across different European countries.
A notable feature is that two of the trials focus on regorafenib, a multikinase inhibitor, suggesting significant interest in this medication as a potential treatment option. The other trials investigate different approaches: OMO-103, which targets the Myc protein involved in cancer cell growth, and denosumab combined with standard chemotherapy, which aims to prevent bone destruction and cancer spread.
The trials include patients ranging from children as young as 9 years old to adults up to 40 years, reflecting the fact that osteosarcoma primarily affects teenagers and young adults. All studies emphasize careful monitoring of safety and effectiveness, with regular assessments using imaging tests and laboratory evaluations. These trials offer hope for patients whose cancer has not responded to conventional treatments or has spread to other parts of the body.