Sg001

Clinical Trials Overview

3 trials found
About Sg001

SG001 is an experimental therapeutic compound that appears to be designed for combination therapy in colorectal cancer treatment. Based on clinical trial data, it is being evaluated alongside hypofractionated radiotherapy and PD-1 antibody therapy for locally recurrent rectal cancer. The drug represents a novel approach to enhancing treatment responses in advanced colorectal cancer patients who have limited therapeutic options.

Category Other Medications
Brand Name Not yet branded
Mechanism The specific molecular mechanism of SG001 has not been fully disclosed in available clinical data. Given its use in combination with PD-1 inhibitors and radiation therapy, it likely functions as an immune system modulator or sensitizing agent that enhances the efficacy of concurrent treatments.
3
Total Trials
1
Recruiting
0
Active
1
Completed
314
Total Enrollment
1
Countries
Active sites for Sg001
Recruiting sites 1 countries
Phase:
NCT07183865 Phase 2 Recruiting 44 patients
Start: Mar 2025
End: Mar 2030
INTERVENTIONAL
This is an open-label, single arm, phase 2 study. The study is to evaluate the activity of combination therapy of hypofractionated radiotherapy, Irinotecan Hydrochloride Liposome plus 5-FU and leucovorin (NALIRIF), Anti-PD1 and target therapy in pati...
China
NCT06132217 Phase 1 Not yet recruiting 168 patients
Start: Jan 2024
End: Jan 2027
INTERVENTIONAL
Medications: SG001 Simmitinib
This is an open-label Phase I/II trial of simmitinib plus SG001 in patients with advanced solid tumors. Phase I will determine and confirm the maximum tolerated dose (MTD) and recommended phase II dose (RP2D) for simmitinib in combination with SG001 ...
China
NCT06089330 Phase 2 Completed 102 patients
Start: Jan 2024
End: Dec 2024
INTERVENTIONAL
This study is a phase Ⅱ, randomized, controlled, open-label, multi-center study with safety run-in to evaluate the efficacy and safety of JMT101 combined with Irinotecan and SG001 in Patients with Metastatic Colorectal Cancer (mCRC).