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SSGJ-709

Phase 1

Advanced Malignant Tumors | Small molecule | Oncology |Sunshine Biopharma Inc.|Last Updated: Jan 28, 2026

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLEDBiomarker
Total Trials1
Total Enrollment15

FDA Designations

No designations recorded

Clinical trial landscape

SSGJ-709 · 1 trial · 1 indication

Phase 1 1
NCT07016490A Phase 1 Study of SSGJ-709 in Patients With Advanced Malignant TumorsAdvanced Malignant Tumors
RECRUITING15 Analytics
PHASE1RECRUITING
A Phase 1 Study of SSGJ-709 in Patients With Advanced Malignant Tumors
Advanced Malignant TumorsUnlock trial analytics

Study Endpoints

Primary Endpoints

Incidence of DLT
21 days

Dose limiting toxicity

Incidence of Treatment-Emergent Adverse Events
through study completion, an average of 1 year

TEAE is any untoward medical occurrence in a participant, temporally associated with the use of study treatment, whether or not considered related to the study treatment.

Secondary Endpoints

Cmax of SSGJ-709
through study completion, an average of 1 year
Tmax of SSGJ-709
through study completion, an average of 1 year
AUC0-last of SSGJ-709
through study completion, an average of 1 year
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Study Design & Arms

AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Experimental: SSGJ-709EXPERIMENTALIn dose escalation phase, SSGJ-709 will be conducted using accelerated titration and traditional 3+3 design. Dose Escalation Level includes 5 levels, Q3W IV. During or after dose escalation, any dose level that does not exceed the MTD can be expanded.

Interventions

NameTypeDescription
SSGJ-709DRUGA bispecific antibody targeting PD-1 and LAG-3.
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites1

Inclusion Criteria: * Minimum life expectancy of 3 months; * Eastern Cooperative Oncology Group (ECOG) Performance status (PS) score of 0-1; * Locally advanced or metastatic malignant tumors confirmed by histopathology or cytology; preferred tumor types for enrollment include head and neck squamous...

Countries:Australia
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Frequently asked questions about SSGJ-709

What is SSGJ-709 used for?

SSGJ-709 is an investigational small molecule being developed for the treatment of advanced malignant tumors. It is currently being studied in a Phase 1 clinical trial in patients with advanced malignant tumors. The drug is not yet approved and remains in clinical development.

What does SSGJ-709 target?

SSGJ-709 is a small molecule therapeutic being developed for oncology. The specific molecular target of SSGJ-709 has not been disclosed in the available information. The drug is currently in Phase 1 clinical development for advanced malignant tumors.

Who makes SSGJ-709?

SSGJ-709 is being developed by Sunshine Biopharma Inc., a biopharmaceutical company listed on the stock exchange under the ticker symbol SBFM. The company is conducting a Phase 1 clinical trial of SSGJ-709 in patients with advanced malignant tumors.

What phase is SSGJ-709 in?

SSGJ-709 is in Phase 1 clinical development. It is an investigational drug being studied in a Phase 1 trial for advanced malignant tumors. The drug is not FDA approved and is still in the early stages of clinical testing.

What clinical trials is SSGJ-709 in?

SSGJ-709 is being studied in a Phase 1 clinical trial with the identifier NCT07016490. This trial is titled 'A Phase 1 Study of SSGJ-709 in Patients With Advanced Malignant Tumors' and is currently recruiting participants in Australia. The study plans to enroll 15 patients.

Is SSGJ-709 the same as any other drug?

SSGJ-709 is the primary name for this investigational drug being developed by Sunshine Biopharma Inc. No alternative names for SSGJ-709 have been disclosed in the available information. The drug is currently in Phase 1 clinical development for advanced malignant tumors.