Taiho Oncology
Taiho Oncology sponsors 52 registered US clinical trials on ClinicalTrials.gov, 7 of them currently recruiting, and 23 completed. 8 of these trials are in Phase 3-4 (later-stage) and 43 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Acute Myeloid Leukemia, with 4 trials.
Trial Pipeline
52 total, page 1 of 2
A Study of ARC-02 in B-cell NHL
NCT07691606
A Study to Assess the Efficacy and Safety of Zipalertinib Versus Placebo for Adjuvant Treatment in Participants With Stage IB-IIIA NSCLC With Uncommon EGFR Mutations, Following Complete Tumor Resection
NCT07128199
A Study of Zipalertinib in Patients With Advanced Non-Small Cell Lung Cancer With Epidermal Growth Factor Receptor (EGFR) Exon 20 Insertions or Other Uncommon Mutation.
NCT05967689
Study of Futibatinib in Patients With Advanced Cholangiocarcinoma With FGFR2 Fusion or Rearrangement
NCT05727176
Study to Evaluate the Pharmacokinetics and Safety of Oral Decitabine and Cedazuridine in Cancer Patients With Hepatic Impairment
NCT04953910
Study to Evaluate the Pharmacokinetics and Safety of Oral Decitabine and Cedazuridine in Cancer Patients With Renal Impairment
NCT04953897
A Multi-phase Study of ASTX030 (Azacitidine and Cedazuridine) in Myeloid Neoplasm Alone or in Combination With Venetoclax in AML (AZTOUND Study)
NCT04256317
REZILIENT3 (REsearching ZIpaLertinib In Egfr Non-small Cell Lung Cancer Tumors)
NCT05973773
Phase 2 Futibatinib in Combination With PD-1 Antibody Based Standard of Care in Solid Tumors
NCT05945823
A Study of Tolinapant in Combination With Oral Decitabine/Cedazuridine and Oral Decitabine/Cedazuridine Alone in Participants With Relapsed/Refractory Peripheral T-cell Lymphoma (R/R PTCL)
NCT05403450
Pharmacokinetics, Safety, and Efficacy of ASTX727 in Combination With Venetoclax in Acute Myeloid Leukemia (AML)
NCT04657081
Phase 1-2 Study of ASTX660 in Subjects With Advanced Solid Tumors and Lymphomas
NCT02503423
A Study of TAS3351 in NSCLC Patients With EGFRmt
NCT05765734
Phase 1b/2 Study of Futibatinib in Combination With Binimetinib in Patients With Advanced KRAS Mutant Cancer
NCT04965818
A Study of TAS2940 in Participants With Locally Advanced or Metastatic Solid Tumor Cancer
NCT04982926
TAS-117 in Patients With Advanced Solid Tumors Harboring Germline PTEN Mutations
NCT04770246
Futibatinib and Pembrolizumab Combination in the Treatment of Advanced or Metastatic Urothelial Carcinoma
NCT04601857
Futibatinib Versus Gemcitabine-Cisplatin Chemotherapy as First-Line Treatment of Patients With Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangements
NCT04093362
Phase III Study of Trifluridine/Tipiracil With and Without Bevacizumab in Refractory Metastatic Colorectal Cancer Patients
NCT04737187
A Study of TAS0612 in Participants With Advanced or Metastatic Solid Tumor Cancer
NCT04586270
Futibatinib in Patients With Specific FGFR Aberrations
NCT04189445
A Study of TAS1440 With ATRA in Subjects With r/r AML
NCT04282668
A Study of TAS-120 in Patients With Metastatic Breast Cancer
NCT04024436
Study of ASTX295 in Patients With Solid Tumors With Wild-Type p53
NCT03975387
Phase 1-2 Study of Low Dose ASTX727 (ASTX727 LD) in Lower Risk MDS
NCT03502668
Study of ASTX029 in Subjects With Advanced Solid Tumors
NCT03520075
A Study of TAS0728 in Patients With Solid Tumors With HER2 or HER3 Abnormalities
NCT03410927
A Study of TAS-116 in Patients With Solid Tumors
NCT02965885
The CHOICE Registry
NCT03148093
A Dose Finding Study Followed by a Safety and Efficacy Study for Patients With Multiple Myeloma or Lymphoma
NCT02978235
A Study Evaluating TAS-102 Plus Nivolumab in Patients With MSS CRC
NCT02860546
A Randomized Phase 2 Trial of TAS-114 in Combination With S-1 Versus S-1
NCT02855125
Study of TAS3681 in Metastatic Castration Resistant Prostate Cancer
NCT02566772
Study of TAS-102 or Placebo Plus BSC in Patients With Metastatic Gastric Cancer
NCT02500043
A Phase I Study of TAS-102 in Patients With Advanced Solid Tumors With Renal Impairment
NCT02301117
A Phase I Study of TAS-102 in Patients With Advanced Solid Tumors With Hepatic Impairment
NCT02301104
An Investigation of TAS-119 Monotherapy
NCT02448589
Dose-escalating, Safety, Tolerability and PK Study of TAS-119 in Combination With Paclitaxel in Patients With Advanced Solid Tumors
NCT02134067
A Study of TAS-120 in Patients With Advanced Solid Tumors
NCT02052778
Study of the Mass Balance of Oral FTD and TPI as Components of TAS-102 in Patients With Advanced Solid Tumors
NCT02031055
A Phase I Study of TAS-102 in Patients With Advanced Gastrointestinal Tumors.
NCT01916447
Study Comparing the Bioavailability of TAS-102 Tablets to an Oral Solution Containing Equivalent Amounts of FTD and TPI
NCT01874522
Study to Evaluate the Cardiac Safety of TAS-102 in Patients With Advanced Solid Tumors
NCT01867879
Study Comparing the Pharmacokinetics of FTD as a Component of TAS-102 With FTD Alone
NCT01867866
A Safety, Tolerability and Pharmacokinetic Study of TAS-114 in Combination With Capecitabine in Patients With Advanced Solid Tumors
NCT02025803
Study of TAS-102 in Patients With Metastatic Colorectal Cancer Refractory to Standard Chemotherapies
NCT01607957
Diffuse Gastric and Esophagogastric Junction Cancer S-1 Trial
NCT01285557
A Phase 1, Open-Label, Randomized, Cross-Over, Pharmacokinetic Study Evaluating the Effect of S-1 on Advanced Solid Tumors
NCT00400023
Evaluating Patients With Impaired Hepatic Function
NCT00398424
Evaluating Patients With Varying Degrees of Renal Function
NCT00398307
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 34 |
| Phase 2 | 9 |
| Phase 3 | 8 |
Therapeutic Areas
What the Pipeline for Taiho Oncology Shows
According to the ClinicalTrials.gov registry, Taiho Oncology is linked to 52 US clinical trials across every stage of research activity. Of those, 7 studies are currently recruiting, about 13% of the sponsor's indexed portfolio, and 23 are already marked complete, representing roughly 44% of the total.
The phase mix for Taiho Oncology reports 8 late-stage studies (Phase 3 and Phase 4 combined) and 43 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Taiho Oncology is Acute Myeloid Leukemia with 4 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.