The disclosure relates to methods, compounds for use and medicaments for the treatment of cancer comprising administering to a subject in need thereof a first agent in a therapeutically effective amount and one or more second agents each in a therapeutically effective amount. In some embodiments, the first agent comprises an EZH2 inhibitor. In certain embodiments, the first agent is tazemetostat or a pharmaceutically acceptable salt thereof and the methods of the disclosure are used to treat lung cancer, e.g., non-small cell lung cancer.

The disclosure relates to methods, compounds for use and medicaments for the treatment of cancer comprising administering to a subject in need thereof a first agent in a therapeutically effective amount and one or more second agents each in a therapeutically effective amount. In some embodiments, the first agent comprises an EZH2 inhibitor. In certain embodiments, the first agent is tazemetostat or a pharmaceutically acceptable salt thereof and the methods of the disclosure are used to treat lung cancer, e.g., non-small cell lung cancer.

The present disclosure provides a dual-drag-containing nanoparticle, in which a first antiviral drag, such as remdesivir and a second antiviral drag are co-encapsulated and co-delivered by the nanoparticle, said nanoparticle comprising an alginate-oleic acid particle. The disclosure also relates to the therapeutic use of the nanoparticle in treating viral infections, such as SARS-CoV-2.

The present disclosure provides a dual-drag-containing nanoparticle, in which a first antiviral drag, such as remdesivir and a second antiviral drag are co-encapsulated and co-delivered by the nanoparticle, said nanoparticle comprising an alginate-oleic acid particle. The disclosure also relates to the therapeutic use of the nanoparticle in treating viral infections, such as SARS-CoV-2.

The present disclosure provides a dual-drag-containing nanoparticle, in which a first antiviral drag, such as remdesivir and a second antiviral drag are co-encapsulated and co-delivered by the nanoparticle, said nanoparticle comprising an alginate-oleic acid particle. The disclosure also relates to the therapeutic use of the nanoparticle in treating viral infections, such as SARS-CoV-2.

A nicotinamide adenine dinucleotide (NAD) precursor is provided for use in the treatment and/or prevention of an age-related medical condition in a subject. The NAD precursor is administered in combination with a calorie restriction diet (CRD) and/or a calorie restriction mimetic (CRM). Furthermore, a pharmaceutical combination is provided that includes a NAD precursor and a CRM.

A nicotinamide adenine dinucleotide (NAD) precursor is provided for use in the treatment and/or prevention of an age-related medical condition in a subject. The NAD precursor is administered in combination with a calorie restriction diet (CRD) and/or a calorie restriction mimetic (CRM). Furthermore, a pharmaceutical combination is provided that includes a NAD precursor and a CRM.

A nicotinamide adenine dinucleotide (NAD) precursor is provided for use in the treatment and/or prevention of an age-related medical condition in a subject. The NAD precursor is administered in combination with a calorie restriction diet (CRD) and/or a calorie restriction mimetic (CRM). Furthermore, a pharmaceutical combination is provided that includes a NAD precursor and a CRM.

The invention concerns a compound of formula (I) and/or a compound of formula (Ia) for use in the prevention and/or treatment of ankylosing spondylitis, as well as compositions and combination preparations comprising them.

The invention concerns a compound of formula (I) and/or a compound of formula (Ia) for use in the prevention and/or treatment of ankylosing spondylitis, as well as compositions and combination preparations comprising them.