| NCT ID | Title | Phase | Status | Enrollment | Velocity | Design | Start | Completion | Last Updated | Sites | Countries |
|---|---|---|---|---|---|---|---|---|---|---|---|
| NCT01514188 | Preliminary Efficacy and Safety of INNO-206 Compared to Doxorubicin in Advanced Soft Tissue Sarcoma | PHASE2 | COMPLETED | 126 | — | — | Jan 11, 2012 | Dec 15, 2014 | May 29, 2024 | 34 | United States, Australia +5 |
Progression-free survival is defined as the interval from the date of registration (ie, assignment of subject number) to the earliest date of documented evidence of recurrent or progressive disease, or the date of death due to any cause, whichever occurs first. Progressive Disease is defined as: 20% increase in the sum of the longest diameter of target lesions from the smallest sum of the longest diameter recorded since the treatment started; the sum must also demonstrate an absolute increase of at least 5 mm. The appearance of 1 new lesion is also considered progression.
| Arm | Type | Description |
|---|---|---|
| Doxorubicin | ACTIVE_COMPARATOR | - |
| INNO-206 | EXPERIMENTAL | - |
| Name | Type | Description |
|---|---|---|
| INNO-206 | DRUG | INNO-206 administered at 350 mg/m2 (260 mg/m2 doxorubicin equivalent) intravenously (IV) on Day 1 every 21 days for up to 6 consecutive cycles |
| Doxorubicin | DRUG | Doxorubicin administered at 75 mg/m2 for up to 6 consecutive cycles. |
Inclusion Criteria: * Age between 15-80 years (US only), and 18-80 (rest of world (ROW)), male or female. * Adjuvant or neoadjuvant chemotherapy (including doxorubicin) allowed if no tumor recurrence for at least 12 months since the last measurement, beginning or end of last chemotherapy. * Histolo...