How do the experts see the potential for fixed-duration combination treatments playing out in first-line CLL therapy? Why do KOLs say AstraZeneca's Calquence + AbbVie/Roche's Venclexta combination is important? What opportunities lie ahead for BeiGene's Brukinsa? How do KOLs assess the potential of BTK degraders such as Nurix's NX-5948 and BeiGene's BGB-16673? KOLs critically assess the prospects of launched and pipeline therapies.
Table of Contents
Executive summary (11)
Current and future treatment algorithm
Research objectives (2)
Bruton's tyrosine kinase (BTK) inhibitors/degraders (66)
- Approved BTK inhibitors (46)
- Imbruvica (ibrutinib; AbbVie/J&J) (11)
- Calquence (acalabrutinib; AstraZeneca) (11)
- Brukinsa (zanubrutinib; BeiGene) (9)
- Jaypirca (pirtobrutinib; Lilly) (15)
- Pipeline BTK inhibitors and degraders (20)
- Nemtabrutinib (Merck & Co.) (10)
- NX-5948, NX-2127 (Nurix Therapeutics) & BGB-16673 (BeiGene) (10)
Bcl-2 inhibitors (19)
- Approved therapies (10)
- Venclexta/Venclyxto (venetoclax; AbbVie/Roche) (10)
- Pipeline therapies (9)
- Sonrotoclax (BGB-11417; BeiGene) and lisaftoclax (Ascentage Pharma) (9)
CAR T-cell therapies (16)
- Pipeline drugs (16)
- Breyanzi (lisocabtagene maraleucel; Bristol Myers Squibb) (11)
- MB-106 (Mustang Bio) (5)
Bispecific antibodies (8)
- Pipeline drugs (8)
- Epkinly/Tepkinly (epcoritamab; AbbVie/Genmab) and Columvi (glofitamab; Roche) (8)
Future treatment trends (5)
Appendix (4)
- KOL details (4)
- KOLs from North America (1)
- KOLs from Europe (2)