Jacobio Pharma Announces 2024 Annual Results
"2024 is a transforatmive year for Jacobio. We have submitted a New Drug Application (NDA) for the KRAS G12C inhibitor glecirasib and have licensed out the
Development of core clinical stage products
Glecirasib (JAB-21822, KRAS G12C inhibitor) and sitneprotafib (JAB-3312,
- The commercialization and further clinical development in
China of glecirasib and sitneprotafib were licensed to Allist onAugust 30, 2024 . - Non-small cell lung cancer (NSCLC)
- The NDA application of glecirasib monotherapy in second-line and above NSCLC was submitted to the CDE (China Drug Evaluation Center) in
May 2024 and the priority review designation was granted in the same month. Glecirasib is expected to be approved in the first half of 2025. - The Phase III pivotal trial of glecirasib combined with sitneprotafib in front-line NSCLC enrolled the first patient in
China onAugust 7, 2024 .
- The NDA application of glecirasib monotherapy in second-line and above NSCLC was submitted to the CDE (China Drug Evaluation Center) in
- Multi-tumor basket
- The multi-tumor basket registration phase II trial of glecirasib for the treatment of pancreatic cancer, biliary tract cancer, gastric cancer, small bowel cancer, appendiceal cancer and other indications has been initiated in
China . Glecirasib has received orphan drug designation (ODD) from FDA and EMA for pancreatic cancer.
- The multi-tumor basket registration phase II trial of glecirasib for the treatment of pancreatic cancer, biliary tract cancer, gastric cancer, small bowel cancer, appendiceal cancer and other indications has been initiated in
- Colorectal cancer
- The Phase III trial of glecirasib mono or in combination with cetuximab in third line was approved by the CDE in
May 2024
- The Phase III trial of glecirasib mono or in combination with cetuximab in third line was approved by the CDE in
JAB-23E73 (pan-KRAS inhibitor)
- The IND (Investigational New Drug) applications were approved in
China andthe United States inSeptember 2024 - The first patient was enrolled in
November 2024 - The dose escalation phase is expected to be completed in the second half of 2025
JAB-30355 (p53 Y220C activator)
- The IND application of FIH (first-in-human) global trial of JAB-30355 was approved by the FDA in
March 2024 and by the CDE inJune 2024 . - The first patient was enrolled in
July 2024 - The dose escalation is expected to be completed in the second half of 2025
JAB-8263 (BET inhibitor)
- The dose escalation for JAB-8263 in solid tumors and hematologic malignancy were completed in the
U.S. andChina , respectively. The RP2D (phase II recommended doses) was obtained. - Dose expansion in patients with myelofibrosis is ongoing.
- Solid tumor portion with specific biomarkers is being explored. .
JAB-2485 (Aurora A inhibitor)
- A Phase I/IIa global trial of JAB-2485 is ongoing in the
U.S. andChina . - Dose escalation phase is expected to be completed in the first half of 2025
- The expansion of monotherapy and combination with chemotherapy are being planned.
Development of pre-clinical pipelines
JAB-BX467 (HER2-
- Clinical candidate of HER2-
STING iADC has been nominated in the second half of 2024. - The IND application is being planned to be submitted in 2026.
JAB-BX600 (KRAS G12D ADC)
- The clinical candidate is expected to be nominated in the second half of 2025.
As of
Conference call information
Jacobio Pharma will hold a conference call at
About Jacobio Pharma
Jacobio Pharma (1167.HK) is committed to providing breakthrough treatments for patients. With an induced allosteric drug discovery platform, the company's core projects focus on the KRAS pathway. The company envisions becoming a global leader in research and development, fostering strategic partnerships to drive innovation. Jacobio's R&D centers are located in
View original content:https://www.prnewswire.com/news-releases/jacobio-pharma-announces-2024-annual-results-302405914.html
SOURCE Jacobio Pharma
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