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INNO-206

Phase 2

Metastatic Soft Tissue Sarcoma | Small molecule | Oncology |ImmunityBio, Inc.|Last Updated: May 29, 2024

Success Probability
Approval Probability 71%
TA Base Rate26%
Adjusted LOA41%
ML RiskLOW_RISK
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Market & Valuation
rNPV $3.2B
Market Size $9.4B
Revenue Basis $1.6B
Competitors 6
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Trial Design
RandomizedACTIVE_CONTROLLEDDMCBiomarker
Total Trials1
Total Enrollment126
FDA Designations
No designations recorded
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT01514188Preliminary Efficacy and Safety of INNO-206 Compared to Doxorubicin in Advanced Soft Tissue SarcomaPHASE2 COMPLETED 126Jan 11, 2012Dec 15, 2014May 29, 202434 United States, Australia +5
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Study Endpoints
Primary Endpoints
Progression-free Survival
Approximately 24 months

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.

Secondary Endpoints
Overall Survival
Approximately 35 months
Progression-free Survival at 4 and 6 Months
Month 4 and 6
Objective Overall Response Rate (ORR)
Approximately 24 months
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Study Design & Arms
AllocationRANDOMIZED
MaskingNONE
ModelPARALLEL
PurposeTREATMENT
Treatment Arms
ArmTypeDescription
DoxorubicinACTIVE_COMPARATOR -
INNO-206EXPERIMENTAL -
Interventions
NameTypeDescription
INNO-206DRUGINNO-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
DoxorubicinDRUGDoxorubicin administered at 75 mg/m2 for up to 6 consecutive cycles.
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Eligibility Criteria
Age Range15 Years — 80 Years
SexALL
Healthy VolunteersNo
Study Sites34

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...

Countries:United StatesAustraliaHungaryIndiaRomaniaRussiaUkraine
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