A61K31/537

PYRIDINYL INDOLE COMPOUNDS AND METHODS OF USE THEREOF

Provided herein are compounds for the treatment or prevention of AMPK-(5′ adenosine monophosphate-activated protein kinase) mediated diseases. Also provided are pharmaceutical compositions comprising the compounds and methods of using the compounds and compositions.

PYRIDINYL INDOLE COMPOUNDS AND METHODS OF USE THEREOF

Provided herein are compounds for the treatment or prevention of AMPK-(5′ adenosine monophosphate-activated protein kinase) mediated diseases. Also provided are pharmaceutical compositions comprising the compounds and methods of using the compounds and compositions.

Methods and systems for conditioning of particulate crystalline materials

Methods and systems for the preparation of conditioned micronized active agents. Additionally, methods and systems for in-process conditioning of micronized active agent particles and compositions comprising conditioned micronized materials.

Methods and systems for conditioning of particulate crystalline materials

Methods and systems for the preparation of conditioned micronized active agents. Additionally, methods and systems for in-process conditioning of micronized active agent particles and compositions comprising conditioned micronized materials.

Pharmaceutical compositions comprising macrolide diastereomers, methods of their synthesis and therapeutic uses

The disclosure relates to compositions comprising diastereomer of a macrolide exhibiting improved therapeutic profile in the context of inhibiting cell proliferation compared to the corresponding compositions comprising mixture of diastereomers. The disclosure further provides drug-ligand conjugates formed using diastereomer of the macrolide. The disclosure also provides novel method of preparation of diastereomer of the macrolide and their therapeutic uses.

Pharmaceutical compositions comprising macrolide diastereomers, methods of their synthesis and therapeutic uses

The disclosure relates to compositions comprising diastereomer of a macrolide exhibiting improved therapeutic profile in the context of inhibiting cell proliferation compared to the corresponding compositions comprising mixture of diastereomers. The disclosure further provides drug-ligand conjugates formed using diastereomer of the macrolide. The disclosure also provides novel method of preparation of diastereomer of the macrolide and their therapeutic uses.

MAYTANSINOID DERIVATIVES, CONJUGATES THEREOF, AND METHODS OF USE
20230116771 · 2023-04-13 ·

Provided herein are maytansinoid compounds, derivatives thereof, conjugates thereof, and methods of treating or preventing proliferative diseases with the same.

MAYTANSINOID DERIVATIVES, CONJUGATES THEREOF, AND METHODS OF USE
20230116771 · 2023-04-13 ·

Provided herein are maytansinoid compounds, derivatives thereof, conjugates thereof, and methods of treating or preventing proliferative diseases with the same.

TISSUE FACTOR-TARGETED ANTIBODY-DRUG CONJUGATE

A tissue factor (TF)-targeted antibody-drug conjugate (ADC) and a method for preparing the ADC. The ADC is capable of binding to TF antigen with high specificity, and has high affinity, low immunogenicity, high cytotoxicity, and significant anti-tumor activity.

TISSUE FACTOR-TARGETED ANTIBODY-DRUG CONJUGATE

A tissue factor (TF)-targeted antibody-drug conjugate (ADC) and a method for preparing the ADC. The ADC is capable of binding to TF antigen with high specificity, and has high affinity, low immunogenicity, high cytotoxicity, and significant anti-tumor activity.