LEADING THE WAY IN ANTI-CANCER DRUG DISCOVERY & DEVELOPMENT

Over the past several decades, Taiho has had a successful track record of producing anti-cancer treatments. These successes have brought us to where we are today, with a strong vision to lead the charge in combining conventional and targeted agents. Our unique two-pronged approach of continuously leveraging expertise in anti-metabolite therapies while also combining them with molecular targeted agents, has uncovered a wide range of potentially promising treatments for the future.

The content listed here is representative of US-based studies. For a full listing of all Taiho studies globally, please see the following:

Taiho Pharmaceutical Company

COMPOUND/MOA COMPOUND/MOA INDICATION DEVELOPMENT STAGE Links

1FUTIBATINIB

Fibroblast growth factor receptor (FGFR) 1-4 inhibitor

Cholangiocarcinoma that has progressed after at least one prior line of systemic therapy

FILED

1FUTIBATINIB

Fibroblast growth factor receptor (FGFR) 1-4 inhibitor

Urothelial Cancer in Combination With Pembrolizumab

Phase 2

1FUTIBATINIB

Fibroblast growth factor receptor (FGFR) 1-4 inhibitor

Solid Tumors in combination with pembrolizumab

Phase 2

2ASTX727 Decitabine and Cedazuridine

Oral DNA methyltransferase inhibitor

Lower Risk MDS

Phase 2

2ASTX727 Decitabine and Cedazuridine

Oral DNA methyltransferase inhibitor

Acute Myeloid Leukemia in combination with venetoclax

Phase 2

Zipalertinib

Tyrosine Kinase Inhibitor

of EGFR exon 20 insertion mutations

Non-Small Cell Lung Cancer 1L

Phase 3

Zipalertinib

Tyrosine Kinase Inhibitor of EGFR exon 20 insertion mutations

Non-Small Cell Lung Cancer 2L+

Phase 2

ASTX030 Azacitidine and Cedazuridine

Oral DNMT inhibitor


Hematological Malignancies

Phase 1

TAS0612

Small molecule triple kinase inhibitor of RSK1,2,3,4, AKT1,2,3 and S6K1,2

Solid Tumours

Phase 1

TAS2940

Covalent pan-ERBB inhibitor with high potency against HER2/EGFR exon20 insertion

Solid Tumours

Phase 1

TAS3351

4th Generation EGFR-TKI

Non-Small Cell Lung Cancer

Phase 1

All data is current as of June 30, 2024.

* This material contains information regarding investigational agents that, unless otherwise indicated have not been approved for commercial use by any country's Regulatory Authority. The efficacy and safety for these investigational agents has not been established. There is no guarantee that these compounds will become commercially available or proven safe and effective for any particular therapeutic indication.

1Futibatinib is approved in the following countries/regions: US, EU, UK, Japan. Please see local labeling for more information.

2 Decitabine/cedazuridine is approved in the following countries/regions: US, Canada, Australia, EU, UK. Please see local labeling for more information.