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Priya Life Science Sponsor trial record
Sponsor · clinical trials

Taiho Oncology clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine and the EU Clinical Trials Information System (CTIS) — current trials in our USA, Spain, France, Italy, Poland, Canada, UK, Germany, South Korea, Japan, Australia, Belgium, Turkey, Brazil, Netherlands, Mexico, Singapore, Israel, Czechia, Austria, China, Portugal and EU (CTIS) registers with Taiho Oncology as lead sponsor. Synced 11 Nov 2026
14Current trials
7Recruiting now
15Drugs in these trials
23Trial registers
At a glance

Taiho Oncology is the lead sponsor of 14 current clinical trials in our USA, Spain, France, Italy, Poland, Canada, UK, Germany, South Korea, Japan, Australia, Belgium, Turkey, Brazil, Netherlands, Mexico, Singapore, Israel, Czechia, Austria, China, Portugal and EU (CTIS) registers. 7 are recruiting patients now. The most common phase is Phase 2. The drugs named most often in its trials are Decitabine, Futibatinib and Zipalertinib. The most-studied condition is Acute Myeloid Leukemia.

ClinicalTrials.gov trials by status

  • Recruiting754%
  • Active, closed538%
  • By invitation18%

Trials by phase

  • Phase 2431%
  • Phase 1323%
  • Phase 3215%
  • Phase 2/3215%
  • Phase 1/2215%
01

Clinical trials sponsored by Taiho Oncology

13 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
Study of Futibatinib in Patients With Advanced Cholangiocarcinoma With FGFR2 Fusion or Rearrangement
NCT05727176 · Advanced Cholangiocarcinoma, FGFR2 Fusions, Gene Rearrangement
Phase 2 Recruiting 2023-07 USA, China, Spain, Italy, Poland, Portugal, Canada, Brazil, Japan, South Korea, Australia
A Study of ARC-02 in B-cell NHL
NCT07691606 · B-cell Non Hodgkin Lymphoma
Drug: Rituximab
Phase 1 Recruiting 2026-06 USA, France, Spain, Italy, Poland, Australia
Study to Evaluate the Pharmacokinetics and Safety of Oral Decitabine and Cedazuridine in Cancer Patients With Hepatic Impairment
NCT04953910 · Acute Myeloid Leukemia, Myelodysplastic Syndromes
Phase 1 Recruiting 2022-12 USA, Spain, Poland
A Multi-phase Study of ASTX030 (Azacitidine and Cedazuridine) in Myeloid Neoplasm Alone or in Combination With Venetoclax in AML (AZTOUND Study)
NCT04256317 · Myelodysplastic Syndromes, Acute Myeloid Leukemia, Myelodysplastic Syndrome/Neoplasm
Phase 2/3 Recruiting 2020-05 UK, USA, Germany, France, Spain, Italy, Poland, Czechia, Canada
A Study to Assess Zipalertinib Versus Placebo in Participants With Early Stage NSCLC With Uncommon EGFR Mutations, Following Complete Tumor Resection
NCT07128199 · Lung Cancer, Adjuvant, Post-surgical
Phase 3 Recruiting 2025-12 UK, USA, Germany, France, Spain, Italy, Netherlands, Belgium, Poland, Turkey, Canada, Brazil, Mexico, Japan, South Korea, Singapore, Australia
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 · Advanced or Metastatic NSCLC Harboring Epidermal Growth Factor Receptor (EGFR) Exon 20 Insertion (ex20ins) Mutations
Phase 2 Recruiting 2023-07 UK, USA, Germany, France, Spain, Italy, Turkey, Canada, Japan, South Korea, Australia, Israel
Study to Evaluate the Pharmacokinetics and Safety of Oral Decitabine and Cedazuridine in Cancer Patients With Renal Impairment
NCT04953897 · Acute Myeloid Leukemia, Myelodysplastic Syndromes
Phase 1 Recruiting 2021-12 USA, Spain, Poland
A Study for Participants Who Participated in Prior Clinical Studies of ASTX727 (Standard Dose)
NCT04093570 · Acute Myeloid Leukemia, Chronic Myelomonocytic Leukemia, Myelodysplastic Syndromes
Phase 2 By invitation 2019-09 USA, Germany, France, Spain, Italy, Poland, Austria, Canada
REZILIENT3 (REsearching ZIpaLertinib In Egfr Non-small Cell Lung Cancer Tumors)
NCT05973773 · Advanced or Metastatic NSCLS With Exon 20 Insertion Mutation
Phase 3 Active, closed 2023-12 UK, USA, Germany, France, Spain, Italy, Netherlands, Belgium, Poland, Turkey, Canada, Brazil, Mexico, Japan, South Korea, Singapore, Israel
Pharmacokinetics, Safety, and Efficacy of ASTX727 in Combination With Venetoclax in Acute Myeloid Leukemia (AML)
NCT04657081 · Acute Myeloid Leukemia
Phase 1/2 Active, closed 2021-02 USA, Spain, Canada
Phase 1-2 Study of ASTX660 in Subjects With Advanced Solid Tumors and Lymphomas
NCT02503423 · Solid Tumors, Lymphoma
Phase 1/2 Active, closed 2015-07 UK, USA, France, Spain, Italy, Belgium, Canada
Futibatinib in Patients Previously Enrolled in an Antecedent Futibatinib as Monotherapy or Combination Therapy.
NCT06506955 · Advanced/Metastatic Cancer
Phase 2/3 Active, closed 2024-10 UK, USA, France, Spain, South Korea
Phase 2 Futibatinib in Combination With PD-1 Antibody Based Standard of Care in Solid Tumors
NCT05945823 · Locally Advanced Unresectable or Metastatic Solid Tumors Including Esophageal Cancer, Esophageal Adenocarcinoma, Esophageal Squamous Cell Cancer
Phase 2 Active, closed 2023-07 USA, Germany, France, Spain

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.

02

Taiho Oncology in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System with Taiho Oncology as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.

StudyPhaseStatusCountries
A Study of ARC-02 in B-cell NHL
2026-525606-35-00 · CTIS ↗ · Neoplasms
Phase 1 Authorised Spain, Poland, France + 1 more
03

Drugs in Taiho Oncology trials

15 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

04

Conditions in Taiho Oncology trials

21 conditions
Acute Myeloid Leukemia5Myelodysplastic Syndromes4Chronic Myelomonocytic Leukemia2Advanced or Metastatic NSCLS With Exon 20 Insertion Mutation1Advanced or Metastatic NSCLC Harboring Epidermal Growth Factor Receptor (EGFR) Exon 20 Insertion (ex20ins) Mutations1Myelodysplastic Syndrome/Neoplasm1Lung Cancer1Adjuvant1Post-surgical1EGFR1Solid Tumors1Lymphoma1Advanced/Metastatic Cancer1B-cell Non Hodgkin Lymphoma1Locally Advanced Unresectable or Metastatic Solid Tumors Including Esophageal Cancer1Esophageal Adenocarcinoma1Esophageal Squamous Cell Cancer1Siewert Type 1 GEJ Cancer1Advanced Cholangiocarcinoma1FGFR2 Fusions1Gene Rearrangement1
07

Questions about Taiho Oncology trials

How many clinical trials does Taiho Oncology sponsor?

Taiho Oncology is the lead sponsor of 13 current trials on ClinicalTrials.gov in our USA, Spain, France, Italy, Poland, Canada, UK, Germany, South Korea, Japan, Australia, Belgium, Turkey, Brazil, Netherlands, Mexico, Singapore, Israel, Czechia, Austria, China and Portugal registers, and 1 authorised or ongoing trial in the EU register (CTIS), as of the registry sync on 11 November 2026. Completed and withdrawn studies are not counted.

Are Taiho Oncology trials recruiting?

Yes. 7 of its 13 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Taiho Oncology testing?

Its current trials name 15 drugs and biologicals as interventions. The most frequent are Decitabine (4), Futibatinib (3), Zipalertinib (3), Venclexta (2) and Venetoclax (2). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 11 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.