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Certepetide Development Pipeline: Targeting Advanced Solid Tumors
Our robust product development pipeline is built on a portfolio of proprietary and patented technology. Driven by Lisata’s vision and mission, our pipeline programs are grounded in rational science to identify and treat patients most likely to respond to our targeted therapies. Click on each program to learn more.
CendR Platform® Programs
The CendR Platform® incorporates novel technologies to enable more effective tumor-targeted, tissue penetrating delivery of anti-cancer agents to advanced solid tumors. The CendR Platform® can also target non-cancerous, immunosuppressive cells selectively within the tumor to enable a patient’s immune system and/or immunotherapies to fight cancer more effectively.
| Indication | Pre Clinical | Phase 1 | Phase 2 | Phase 3 |
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Indication: First-Line Metastatic Pancreatic Ductal Adenocarcinoma (mPDAC) |
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| ASCEND: Gemcitabine/Nab-paclitaxel with certepetide or placebo | Australia/New Zealand | ||||
| First-Line Metastatic Pancreatic Ductal Adenocarcinoma (mPDAC) |
ASCEND: Gemcitabine/Nab-paclitaxel with certepetide or placebo | Australia/New Zealand
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Phase 2
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| Phase 1b/2a: Gemcitabine/Nab-paclitaxel + certepetide | China | ||||
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Phase 1b/2a: Gemcitabine/Nab-paclitaxel + certepetide | China
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Phase 1
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| iLSTA: Gemcitabine/Nab-paclitaxel/Durvalumab + certepetide | Australia | ||||
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iLSTA: Gemcitabine/Nab-paclitaxel/Durvalumab + certepetide | Australia
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Phase 1
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| Phase 2b: Gemcitabine/Nab-paclitaxel + certepetide | China | ||||
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Phase 2b: Gemcitabine/Nab-paclitaxel + certepetide | China
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Phase 2
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| FORTIFIDE: Gemcitabine/Nab-paclitaxel + continuous infusion of certepetide or placebo | United States | ||||
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FORTIFIDE: Gemcitabine/Nab-paclitaxel + continuous infusion of certepetide or placebo | United States
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Phase 1
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Indication: Pancreatic, Colon, and Appendiceal Cancers |
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| CENDIFOX: FOLFIRINOX + panitumumab with certepetide | United States | ||||
| Pancreatic, Colon, and Appendiceal Cancers |
CENDIFOX: FOLFIRINOX + panitumumab with certepetide | United States
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Phase 1
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Indication: Cholangiocarcinoma (CCA) |
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| BOLSTER: Gemcitabine/Cisplatin/Durvalumab with certepetide or placebo | United States | ||||
| Cholangiocarcinoma (CCA) |
BOLSTER: Gemcitabine/Cisplatin/Durvalumab with certepetide or placebo | United States
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Phase 2
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Indication: Glioblastoma Multiforme |
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| Temozolomide with certepetide or placebo | Estonia/Latvia | ||||
| Glioblastoma Multiforme |
Temozolomide with certepetide or placebo | Estonia/Latvia
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Phase 2
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Certepetide has been awarded Fast Track designation (U.S.) and Orphan Drug Designation for pancreatic cancer (U.S. and E.U.) as well as Orphan Drug Designation for glioma, osteosarcoma, and cholangiocarcinoma (U.S.). Additionally, certepetide has received Rare Pediatric Disease Designation for osteosarcoma (U.S.).