Drug intelligence / Profile preview

ABTL0812 + gemcitabine + nab-paclitaxel

Development stage
Phase 2
Lead developer
AbilityPharma
Modality
Small Molecules, Nanoparticles → Drug Delivery Systems
Administration
Oral (ABTL0812), Intravenous (gemcitabine), Intravenous (nab-paclitaxel)
01

Overview

ABTL0812 + gemcitabine + nab-paclitaxel is a combination regimen under clinical investigation for cancer, specifically pancreatic cancer. ABTL0812 is a first-in-class, orally administered small molecule developed by AbilityPharma that induces cytotoxic autophagy in cancer cells by a dual mechanism: (1) inhibition of the Akt/mTORC1 pathway via upregulation of TRIB3 pseudokinase (itself driven by activating PPARα and PPARγ), and (2) induction of endoplasmic reticulum (ER) stress, leading to activation of the unfolded protein response. These converge to drive robust autophagy and cancer cell death. Gemcitabine is a nucleoside analog (antimetabolite) and standard chemotherapy, while nab-paclitaxel is a nanoparticle albumin-bound formulation of the antitubulin agent paclitaxel, providing enhanced delivery and antineoplastic activity. This combination is primarily being evaluated in advanced or metastatic pancreatic cancer in clinical trials, with rationale based on synergistic anticancer effects and the ability of ABTL0812 to overcome chemoresistance and augment standard chemotherapy efficacy[1][3][6].

Brand names
None specific to the combinationAbraxane (nab-paclitaxel brand)Gemzar (gemcitabine brand, not specific to combo)
Other names
ABTL0812 plus gemcitabine plus nab-paclitaxelABTL-0812 plus gemcitabine plus nab-paclitaxelABTL 0812 plus gemcitabine plus nab-paclitaxelABTL0812 combined with gemcitabine and nanoparticle albumin-bound paclitaxelABTL-0812 combined with gemcitabine and nanoparticle albumin-bound paclitaxelABTL 0812 combined with gemcitabine and nanoparticle albumin-bound paclitaxel
02

Targets

DNA polymerase familyPPARA (Peroxisome proliferator-activated receptor alpha)PPARG (Peroxisome proliferator-activated receptor gamma)RNR (Ribonucleotide reductase)AKT (RAC-alpha serine/threonine-protein kinase)Mechanistic target of rapamycin complex 1TUBB (Tubulin (alpha and beta subunits))

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