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Phase 2 N=51 Diagnostic

A Study to Evaluate ONM100, an Intraoperative Fluor Imaging Agent for the Detection of Peri Mets

Peritoneal Carcinomatosis

Enrolled (actual)
51
Serious AEs
34.0%
Results posted
Nov 2024
Primary outcome: Primary: Percentage of Patients That Had at Least One Additional Lesion Detected Under Pegsitacianine Guidance Following CRS That Was Confirmed as Positive for Disease by Pathological Evaluation — 20 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
pegsitacianine (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
OncoNano Medicine, Inc.
Primary completion
Dec 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Patients That Had at Least One Additional Lesion Detected Under Pegsitacianine Guidance Following CRS That Was Confirmed as Positive for Disease by Pathological Evaluation
20
SECONDARY
Sensitivity of Pegsitacianine at Detecting Presence of Tumor Within the Tissue Specimen
.786
SECONDARY
Specificity of Pegsitacianine at Detecting Presence of Tumor Within the Tissue Specimen
.564
SECONDARY
Negative Predictive Value of Pegsitacianine
.68
SECONDARY
Positive Predictive Value of Pegsitacianine
.689

Summary

Peritoneal carcinomatosis (PC) results from the metastasis of a primary cancer of the peritoneum (e.g., appendiceal, ovarian, uterine, colorectal, and gastric cancers) that then disseminates throughout the abdominal cavity. Historically progression to PC was considered terminal and resulted in survival times on the scale of a few months with palliative care being the best option for patients. More recently, cytoreductive surgery (CS) has emerged as a means to prolong and improve patient lives with a median increase in survival of up to ~5 years. It has been reported that for every 10% increase in cytoreduction there is a 5.5% increase in median survival time. In addition to surgical tumor debulking within the peritoneal space, it has also been shown that coupling surgical intervention with hyperthermic intraperitoneal chemotherapy (HIPEC) can have an even greater impact on patient outcomes. Pegsitacianine, a micellar fluorescence agent, exploits the ubiquitous pH differences observed between cancerous and normal tissues. This in turn, provides a highly sensitive and specific fluorescence response after localizing within the tumor microenvironment, thus allowing the detection of primary tumors, their margins, metastatic disease, and tumor-containing lymph nodes.

Eligibility Criteria

Inclusion Criteria

  • Imaging and biopsy confirmed metastatic disease of peritoneal origin

Exclusion Criteria

  • Known hypersensitivity or allergy to any component of pegsitacianine
  • Tumor locations the surgeon deems unfeasible to image intraoperatively
  • Excessive and/or generalized metastatic disease deemed inoperative by the surgeon
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04950166). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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