Synergistic auristatin combinations
This invention relates to combinations of an auristatin or an auristatin-based antibody-drug-conjugate (ADC) with second active agents including PI3K/mTOR inhibitors, MEK inhibitors, taxanes, or other anti-cancer agents, and methods of treating abnormal cell growth by administering these combinations to patients.
1. A method for treating lung cancer or breast cancer in a subject, comprising concurrently administering to a subject in need thereof an antibody-drug-conjugate comprising auristatin-101 and a dual-specificity PI3K-mTOR inhibitor which is PF-384.
2. The method of claim 1 , wherein said antibody-drug-coniugate comprising auristatin-101 and said PF-384 are administered simultaneously or are administered in sequence.
3. The method of claim 1 wherein said antibody-drug-conjugate comprising auristatin-101 and said PF-384 are administered sequentially in either order.
4. A pharmaceutical composition for treating lung cancer or breast cancer comprising: an amount of antibody-drug-conjugate comprising auristatin-101 or a pharmaceutically acceptable salt thereof; an amount of a dual-specificity PI3K-mTOR inhibitor which is PF-384 or a pharmaceutically acceptable salt thereof; and a pharmaceutically acceptable carrier or diluent.
5. A dosage form for treating lung cancer or breast cancer in a mammal comprising: (a) antibody-drug-conjugate comprising auristatin-101, or a pharmaceutically acceptable salt thereof; (b) a dual-specificity PI3K-mTOR inhibitor which is PF-384; and (c) a pharmaceutically acceptable carrier or diluent.
6. A kit for treating lung cancer or breast cancer in a mammal, said kit comprising: (a) an antibody-drug-conjugate comprising auristatin-101 or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or diluent in a first unit dosage form; (b) a dual-specificity PI3K-mTOR inhibitor which is PF-384, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or diluent in a second unit dosage form, and (c) means for containing said first and second dosage forms.