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Pipeline

Development Programs – Solid Tumor

Drug

Indication

Phase 1

Phase 2

Phase 3


Tislelizumab

(anti-PD-1)
1L NonSq NSCLC

1L Sq NSCLC

2/3L NSCLC

Neo/adj NSCLC

1L ES-SCLC

1L ESCC

2L ESCC

LA ESCC

1L GC/GEJC

1L NPC

1L HCC

1L UBC

2/3L HCC

1L NSCLC (subcutaneous formulation)

Ociperlimab

(anti-TIGIT)
1L PD-L1 high NSCLC

NSCLC dose confirmation

BG-685011

(CDK2 inhibitor)
BC and solid tumors

BGB-43395

(CDK4 inhibitor)
BC and solid tumors

BG-C90742

(B7H4-ADC)
BC and solid tumors

BGB-C354

(B7H3-ADC)
Solid tumors

LBL-0073

(anti-LAG3)
MSS-CRC

1L ESCC

Umbrella

(IO combinations)
1L NSCLCa

Neo/adj NSCLCa

2L+ NSCLCa

1L HNSCCa

Zanidatamab4

(anti-HER2 BsAb)
2L HER2+ BTC

1L HER2+ GEA

BGB-A445

(anti-OX40)
Melanoma, UC

BGB-15025

(HPK1 inhibitor)
Solid tumors

BGB-26808

(HPK1 inhibitor)
Solid tumors

BGB-24714

(SMAC mimetic)
Solid tumors

BGB-30813

(DGKζ inhibitor)
Solid tumors

BGB-A3055

(anti-CCR8)
Solid tumors

Pamiparib

(PARP 1/2 inhibitor)
2L MTx gBRCAm PSOC

Tarlatamab5

(DLL3 x CD3)
2L SCLC

1L-ES-SCLC

LS-SCLC

3L+ SCLC (initiation activities)

Xaluritamig5

(STEAP1 x CD3)
mCRPC

BGB-R046

(IL-15 prodrug)
Solid tumors

BGB-B3227

(MUC1 x CD16A BsAb)
Lung and GI

BGB-B2033

(GPC3 x 4-1BB)
Solid tumors

BG-C477

(CEA ADC)
Lung and GI cancers (preclinical)

BGB-53038

(PanKRAS inhibitor)
Lung and GI cancers (preclinical)

BG-C137

(FGFR2b ADC)
GI cancer (preclinical)

BGB-58067

(PRMT5 inhibitor)
Lung and GI cancers (preclinical)

BG-60366

(EGFR-targeted CDAC)
Lung cancer (preclinical)

Planned for 2024

Safety and efficacy have not been established for investigational products and/or uses.

Development Programs – Hematology

Drug

Indication

Phase 1

Phase 2

Phase 3


Zanubrutinib

(BTK inhibitor)
CLL/SLL

WM

R/R FL

R/R MZL

TN MCL

R/R MCL

R/R DLBCL with CD79B

Previously treated B-cell malignancies

Sonrotoclax

(BCL2 inhibitor)
TN CLLb

R/R WM

R/R CLL

R/R MCL

R/R MM with t(11;14)

AML/MDS

B-cell malignancies

BGB-16673

(BTK-targeted CDAC)
B-cell malignancies

R/R MCL and R/R CLL

BGB-21447

(BCL2 inhibitor)
B-cell malignancies

Tislelizumab

(anti-PD-1)
R/R cHL

Ociperlimab

(anti-TIGIT)
R/R DLBCL

Zanubrutinib

(BTK inhibitor)
Primary membranous nephropathy

Lupus nephritis

BGB-45035

(IRAK4-targeted CDAC)
Immunology & inflammation

Blinatumomab5

(CD3 X CD19)
Pediatric R/R BP-ALL

Safety and efficacy have not been established for investigational products and/or uses.

aMay include anti-PD-1, anti-LAG3, anti-OX40, and HPK1 inhibitor.
bin combination with Zanubrutinib.

1Ensem collaboration; BeiGene has global rights.
2DualityBio collaboration; BeiGene has global rights.
3Leads Biolabs collaboration; BeiGene has ex-China commercial rights.
4Zymeworks/Jazz collaboration; BeiGene has APAC/ex Japan, AU, and NZ commercial rights.
5Amgen collaboration; BeiGene has China commercial rights.

1L, first line; 2L, second line; 3L, third line; 4-1BB, tumor necrosis factor receptor superfamily member 9; ADC, antibody-drug conjugate; AML, acute myeloid leukemia; BC, breast cancer; BCL2, B-cell lymphoma 2; BsAb, bispecific antibody; BP-ALL, B-cell precursor acute lymphoblastic leukemia; BTC, biliary tract cancer; BTK, Bruton tyrosine kinase; CCR8, the C-C motif chemokine receptor 8; CD3, cluster of differentiation 3; CD16A, Fc receptor FcγRIIIa; CD19, cluster of differentiation 19; CD79B, cluster of differentiation 79B; CDAC, chimeric degradation activating compound; CDK2, cyclin-dependent kinase 2; CDK4, cyclin-dependent kinase 4; CEA, carcinoembryonic antigen; cHL, classical Hodgkin lymphoma; CLL, chronic lymphocytic leukemia; CRC, colorectal cancer; DGKζ, diacylglycerol kinase ζ; DLBCL, diffuse large B-cell lymphoma; DLL3, delta-like ligand 3; EGFR, epidermal growth factor receptor; ESCC, esophageal squamous cell carcinoma; ES-SCLC, extensive-stage small cell lung cancer; FGFR2b, fibroblast growth factor receptor 2, isoform IIIb; FL, follicular lymphoma; gBRCAm, germline BReast CAncer gene (BRCA) mutation; GC, gastric cancer; GEA, gastroesophageal adenocarcinomas; GEJC, gastroesophageal junction carcinoma; GI, gastrointestinal; GPC3, glypican-3; IL-15, interleukin-15; HCC, hepatocellular carcinoma; HER2, human epidermal growth factor receptor 2; HNSCC, head and neck squamous cell carcinoma; HPK1, hematopoietic progenitor kinase 1; IO, immunotherapy; IRAK4, interleukin-1 receptor-associated kinase 4; KRAS, Kirsten rat sarcoma virus; LA, locally advanced; LAG3, lymphocyte activation gene 3; LS-SCLC, limited-stage small cell lung cancer; MCL, mantle cell lymphoma; mCRPC, metastatic castration-resistant prostate cancer; MDS, myelodysplastic syndromes; MM, multiple myeloma; MSS, microsatellite stability; MTx, maintenance treatment; MUC1, mucin 1; PARP 1/2, poly (ADP-ribose) polymerase 1 and 2; MZL, marginal zone lymphoma; NPC, nasopharyngeal carcinoma; NonSq, non-squamous; NSCLC, non–small cell lung cancer; OX40, a member of the tumor necrosis factor (TNF) receptor family, also know as CD134; PD-1, programmed cell death protein 1; PD-L1, programmed death-ligand 1; PRMT5, protein arginine methyltransferase 5; PSOC, platinum-sensitive ovarian cancer; R/R, recurrent/refractory; SCLC, small cell lung cancer; SLL, small lymphocytic lymphoma; SMAC, second mitochondria-derived activator of caspase; STEAP1, six-transmembrane epithelial antigen of the prostate 1; Sq, squamous; TIGIT, T-cell immunoreceptor with Ig and ITIM domains; TN, treatment naive; UBC, urothelial bladder cancer; UC, urothelial carcinoma; WM, Waldenström macroglobulinemia.

Videos

Anti-OX40 Mechanism of Action

Anti-PD-1 Mechanism of Action

CDK4 Inhibitor Mechanism of Action

BTKI Mechanism of Action

Anti-TIGIT Mechanism of Action

PARPI Mechanism of Action