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Jacobio Pharmaceuticals Group Co., Ltd. (HK:1167)
:1167
Jab-23E73
Advanced Solid Tumor
Phase I/II
Recruiting
A Phase I/IIa Study of JAB-23E73 in Patients With Advanced Solid Tumors Harboring KRAS Gene Alteration
Apr 28, 2025
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Jab-23E73
Advanced Solid Tumors
Phase I/II
Not Yet Recruiting
JAB-23E73 in Adult Participants With Advanced Solid Tumors With KRAS Alteration
Apr 24, 2025
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Jab-30355
Solid Tumors
Phase I/II
Recruiting
JAB-30355 in Patients With Advanced Solid Tumors Harboring TP53 Y220C Mutation
Apr 23, 2024
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Jab-3068
Non-small Cell Lung Cancer, Esophageal Cancer, Head And Neck Cancer, Other Metastatic Solid Tumors
Phase I
Completed
A First in Human, Dose Escalation Study of JAB-3068 （SHP2 Inhibitor） in Adult Patients With Advanced Solid Tumors
Apr 06, 2018
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FAQ
What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases:
a. Preclinical testing
b. Phase 1 – Safety and dosage
c. Phase 2 – Effectiveness and side effects
d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments
e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
a. Preclinical testing
b. Phase 1 – Safety and dosage
c. Phase 2 – Effectiveness and side effects
d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments
e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
What is a clinical trial?
A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
What drugs does Jacobio Pharmaceuticals Group Co., Ltd. (1167) have in its pipeline
1167 is currently developing the following drugs: Jab-23E73, Jab-23E73, Jab-30355. These drug candidates are in various stages of clinical development as the company works toward FDA approval.