Taiho Oncology

52 total trials 7 currently recruiting 23 completed

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

RECRUITING Phase 1

A Study of ARC-02 in B-cell NHL

NCT07691606

RECRUITING Phase 3

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

RECRUITING Phase 2

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

RECRUITING Phase 2

Study of Futibatinib in Patients With Advanced Cholangiocarcinoma With FGFR2 Fusion or Rearrangement

NCT05727176

RECRUITING Phase 1

Study to Evaluate the Pharmacokinetics and Safety of Oral Decitabine and Cedazuridine in Cancer Patients With Hepatic Impairment

NCT04953910

RECRUITING Phase 1

Study to Evaluate the Pharmacokinetics and Safety of Oral Decitabine and Cedazuridine in Cancer Patients With Renal Impairment

NCT04953897

RECRUITING Phase 2

A Multi-phase Study of ASTX030 (Azacitidine and Cedazuridine) in Myeloid Neoplasm Alone or in Combination With Venetoclax in AML (AZTOUND Study)

NCT04256317

ACTIVE NOT RECRUITING Phase 3

REZILIENT3 (REsearching ZIpaLertinib In Egfr Non-small Cell Lung Cancer Tumors)

NCT05973773

ACTIVE NOT RECRUITING Phase 2

Phase 2 Futibatinib in Combination With PD-1 Antibody Based Standard of Care in Solid Tumors

NCT05945823

ACTIVE NOT RECRUITING Phase 1

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

ACTIVE NOT RECRUITING Phase 1

Pharmacokinetics, Safety, and Efficacy of ASTX727 in Combination With Venetoclax in Acute Myeloid Leukemia (AML)

NCT04657081

ACTIVE NOT RECRUITING Phase 1

Phase 1-2 Study of ASTX660 in Subjects With Advanced Solid Tumors and Lymphomas

NCT02503423

TERMINATED Phase 1

A Study of TAS3351 in NSCLC Patients With EGFRmt

NCT05765734

TERMINATED Phase 1

Phase 1b/2 Study of Futibatinib in Combination With Binimetinib in Patients With Advanced KRAS Mutant Cancer

NCT04965818

TERMINATED Phase 1

A Study of TAS2940 in Participants With Locally Advanced or Metastatic Solid Tumor Cancer

NCT04982926

TERMINATED Phase 1

TAS-117 in Patients With Advanced Solid Tumors Harboring Germline PTEN Mutations

NCT04770246

TERMINATED Phase 2

Futibatinib and Pembrolizumab Combination in the Treatment of Advanced or Metastatic Urothelial Carcinoma

NCT04601857

TERMINATED Phase 3

Futibatinib Versus Gemcitabine-Cisplatin Chemotherapy as First-Line Treatment of Patients With Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangements

NCT04093362

COMPLETED Phase 3

Phase III Study of Trifluridine/Tipiracil With and Without Bevacizumab in Refractory Metastatic Colorectal Cancer Patients

NCT04737187

TERMINATED Phase 1

A Study of TAS0612 in Participants With Advanced or Metastatic Solid Tumor Cancer

NCT04586270

TERMINATED Phase 2

Futibatinib in Patients With Specific FGFR Aberrations

NCT04189445

TERMINATED Phase 1

A Study of TAS1440 With ATRA in Subjects With r/r AML

NCT04282668

TERMINATED Phase 2

A Study of TAS-120 in Patients With Metastatic Breast Cancer

NCT04024436

TERMINATED Phase 1

Study of ASTX295 in Patients With Solid Tumors With Wild-Type p53

NCT03975387

COMPLETED Phase 1

Phase 1-2 Study of Low Dose ASTX727 (ASTX727 LD) in Lower Risk MDS

NCT03502668

COMPLETED Phase 1

Study of ASTX029 in Subjects With Advanced Solid Tumors

NCT03520075

TERMINATED Phase 1

A Study of TAS0728 in Patients With Solid Tumors With HER2 or HER3 Abnormalities

NCT03410927

COMPLETED Phase 1

A Study of TAS-116 in Patients With Solid Tumors

NCT02965885

TERMINATED

The CHOICE Registry

NCT03148093

TERMINATED Phase 1

A Dose Finding Study Followed by a Safety and Efficacy Study for Patients With Multiple Myeloma or Lymphoma

NCT02978235

COMPLETED Phase 2

A Study Evaluating TAS-102 Plus Nivolumab in Patients With MSS CRC

NCT02860546

COMPLETED Phase 2

A Randomized Phase 2 Trial of TAS-114 in Combination With S-1 Versus S-1

NCT02855125

COMPLETED Phase 1

Study of TAS3681 in Metastatic Castration Resistant Prostate Cancer

NCT02566772

COMPLETED Phase 3

Study of TAS-102 or Placebo Plus BSC in Patients With Metastatic Gastric Cancer

NCT02500043

COMPLETED Phase 1

A Phase I Study of TAS-102 in Patients With Advanced Solid Tumors With Renal Impairment

NCT02301117

COMPLETED Phase 1

A Phase I Study of TAS-102 in Patients With Advanced Solid Tumors With Hepatic Impairment

NCT02301104

TERMINATED Phase 1

An Investigation of TAS-119 Monotherapy

NCT02448589

TERMINATED Phase 1

Dose-escalating, Safety, Tolerability and PK Study of TAS-119 in Combination With Paclitaxel in Patients With Advanced Solid Tumors

NCT02134067

COMPLETED Phase 1

A Study of TAS-120 in Patients With Advanced Solid Tumors

NCT02052778

COMPLETED Phase 1

Study of the Mass Balance of Oral FTD and TPI as Components of TAS-102 in Patients With Advanced Solid Tumors

NCT02031055

COMPLETED Phase 1

A Phase I Study of TAS-102 in Patients With Advanced Gastrointestinal Tumors.

NCT01916447

COMPLETED Phase 1

Study Comparing the Bioavailability of TAS-102 Tablets to an Oral Solution Containing Equivalent Amounts of FTD and TPI

NCT01874522

COMPLETED Phase 1

Study to Evaluate the Cardiac Safety of TAS-102 in Patients With Advanced Solid Tumors

NCT01867879

COMPLETED Phase 1

Study Comparing the Pharmacokinetics of FTD as a Component of TAS-102 With FTD Alone

NCT01867866

COMPLETED Phase 1

A Safety, Tolerability and Pharmacokinetic Study of TAS-114 in Combination With Capecitabine in Patients With Advanced Solid Tumors

NCT02025803

COMPLETED Phase 3

Study of TAS-102 in Patients With Metastatic Colorectal Cancer Refractory to Standard Chemotherapies

NCT01607957

TERMINATED Phase 3

Diffuse Gastric and Esophagogastric Junction Cancer S-1 Trial

NCT01285557

COMPLETED Phase 1

A Phase 1, Open-Label, Randomized, Cross-Over, Pharmacokinetic Study Evaluating the Effect of S-1 on Advanced Solid Tumors

NCT00400023

COMPLETED Phase 1

Evaluating Patients With Impaired Hepatic Function

NCT00398424

COMPLETED Phase 1

Evaluating Patients With Varying Degrees of Renal Function

NCT00398307

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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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.