Condition: Osteogenic Sarcoma Recurrent · Sponsor: Hackensack Meridian Health
This will be a phase II, single arm study of osteosarcoma patients with fully resected pulmonary metastases. The MTD corresponds to the dosage recommendations of the manufacturer of Iscador® P which is licensed in Sweden, New Zealand, South Korea, Germany and Switzerland for the treatment of solid tumors and precancerous lesions. The study population includes patients with relapse of osteosarcoma in the lung following surgical resection of all gross disease (2nd or greater CR). Following completion of final thoracotomy, they will be treated with Iscador® P at concentrations up to the MTD with surveillance imaging via CT scan to monitor for relapsed disease.
This description comes directly from the study's public registry record.
Laura Goode, MS, RN, PCNS-BC · 5519964995 · laura.goode@hmhn.org
Always discuss trial participation with your own doctor first.
| Hackensack University Medical Center | Hackensack, New Jersey, United States | Recruiting |
| M.D. Anderson Children's Cancer Hospital | Houston, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05726383