Clinical trials

17

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

INTREPID: A Study of Sapablursen Evaluating the Safety and Efficacy in Participants With Polycythemia Vera (PV)

The purpose of this study is to evaluate the efficacy and safety of sapablursen when added on to current standard of care (SOC) for Polycythemia Vera (PV) therapy. The study will be conducted in three sequential parts (Part 1a blinded treatment, Part 1b open-label treatment, \& Part 2 long-term extension). Participants may receive treatment for up to 156 weeks.

Participants needed: 250
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Jun 30, 2026Locations: 5
Eligibility criteria

Meet revised 2022 World Health Organization (WHO) and 2022 International Consens... [+4]

Prior treatment of PV with Transmembrane serine protease 6 (TMPRSS6) inhibitors,... [+4]

Status: Recruiting

IGNITE: Study of Tirabrutinib vs Rituximab/Temozolomide for Relapsed/Refractory Primary Central Nervous System Lymphoma (PCNSL)

The purpose of this clinical trial is to evaluate efficacy and safety of tirabrutinib alone compared with rituximab and temozolomide (R-TMZ) combination therapy in participants with Relapsed/Refractory Primary Central Nervous System Lymphoma (PCNSL).

Participants needed: 132
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Jun 25, 2026Locations: 19
Eligibility criteria

Pathology report confirming the diagnosis of B-cell PCNSL [+6]

Participants with isolated intraocular PCNSL or spinal PCNSL with no brain lesio... [+9]

Status: Recruiting

A Study to Evaluate the Safety and Efficacy of Two Dose Levels of ONO-4578 With Opdivo®, in Combination With mFOLFOX6 and Bevacizumab Versus Standard of Care in Participants With Non-MSI-H/dMMR, PD-L1 Positive Advanced Colorectal Cancer

The purpose of this study is to evaluate the safety and efficacy of two dose levels of ONO-4578 with Opdivo® when added to mFOLFOX6 and bevacizumab versus SOC as first-line treatment for advanced CRC.

Participants needed: 144
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Jun 15, 2026Locations: 35
Eligibility criteria

Histologically confirmed advanced (locally advanced or metastatic) colorectal ca... [+3]

Participants with high microsatellite instability (MSI-High), or mismatch repair... [+5]

Status: Recruiting

A Study of ONO-3310 in Healthy Adult Male Subjects and Chronic Kidney Disease Patients With Type 2 Diabetes Mellitus

To investigate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single and multiple oral doses of ONO-3310 in healthy Japanese adult male subjects and chronic kidney disease patients with type 2 diabetes mellitus

Participants needed: 120
Trial details
Phase: Phase 1Age: 18-64Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Jun 8, 2026Locations: 1
Eligibility criteria

Japanese healthy adult male subjects [+5]

Subjects who currently receive treatment for or have a history of any of the fol... [+5]

Status: Not yet recruiting

Study of DCC-2618 in Patients With GIST After at Least 3 Prior Treatments

To evaluate the safety of DCC-2618 in patients with unresectable, metastatic, or recurrent gastrointestinal stromal tumor (GIST) who have received three or more prior therapies

Participants needed: 10
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Jun 1, 2026Locations: 2
Eligibility criteria

Participants with a histologically confirmed diagnosis of GIST. [+3]

Participants with a concomitant or prior history of severe hypersensitivity reac... [+2]

Status: Recruiting

A Retrospective Observational Study of Nivolumab in Combination With Chemotherapy as Neoadjuvant Therapy for Resectable NSCLC Patients: Real-World Experience in Taiwan (NEOREAL)

The goal of this observational study is to learn about the effectiveness of Nivolumab in combination with chemotherapy as Neoadjuvant therapy for patients with non-small cell lung cancer (NSCLC). The main question it aims to answer is: Does patient with NSCLC in treatment of Nivolumab combined with chemotherapy demonstrate better pCR and PFS ? Is it safe for patient with NSCLC in treatment of Nivolumab combined with chemotherapy ? The data for those participants already receiving nivolumab in combination with chemotherapy as part of their regular medical care for NSCLC will be collected within the designated collection period.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ono Pharmaceutical Co., Ltd.Updated: May 20, 2026Locations: 9
Eligibility criteria

Aged 18 years and older [+5]

Patients with distant metastasis (M1 disease according to the eighth edition of... [+4]

Status: Recruiting

A Study to Evaluate the Safety, Efficacy, and PK of ONO-2017 in Japanese Patients With POS 2 to 17 Year Olds

Primary objective: To evaluate the safety and tolerability of cenobamate in Japanese pediatric subjects 2-17 years of age with partial-onset (focal) seizures

Participants needed: 20
Trial details
Phase: Phase 3Age: 2-17Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: May 18, 2026Locations: 1
Eligibility criteria

Japanese male or female patients aged 2 to under 18 years at the time of informe... [+3]

Patients with a history of status epilepticus requiring hospitalization within 3... [+4]

Status: Recruiting

A Study of ONO-2020 in Patients With Agitation Associated With Alzheimer's Disease Dementia

To evaluate the efficacy and safety of ONO-2020 in patients with agitation associated with Alzheimer's Disease dementia in Japan.

Participants needed: 90
Trial details
Phase: Phase 2Age: 55-90Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: May 12, 2026Locations: 38
Eligibility criteria

Diagnosis of probable AD according to the diagnostic criteria for AD dementia (N... [+4]

Diagnosis of dementia not due to AD or any other disorder with memory impairment... [+4]

Status: Recruiting

Study to ONO-4538 in Patients With Rhabdoid Tumor

Investigate the efficacy and safety of ONO-4538 for the treatment of rhabdoid Tumors

Participants needed: 23
Trial details
Phase: Phase 2Age: 1+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Mar 12, 2026Locations: 5
Eligibility criteria

Gender: Not specified [+3]

Patients with a history of active concurrent malignancy or complications [+2]

Status: Recruiting

ONO-4538 Study in Patients With Richter's Transformation

Investigate the efficacy and safety of ONO-4538 in patients with Richter's transformation

Participants needed: 14
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Feb 13, 2026Locations: 10
Eligibility criteria

Histological diagnosis of diffuse large B-cell lymphoma (DLBCL)-type or Hodgkin... [+4]

Serious complications [+3]

Status: Recruiting

Study of ONO-4685 in Patients With Relapsed or Refractory T Cell Lymphoma

This study will investigate the safety, tolerability, pharmacokinetics, and preliminary efficacy of ONO-4685 in patients with relapsed or refractory T cell Lymphoma

Participants needed: 217
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Feb 13, 2026Locations: 20
Eligibility criteria

Patients aged ≥ 18 years at time of screening [+9]

Patients with central nervous system (CNS) involvement [+10]

Status: Recruiting

A Study of ONO-7428 in Participants With Unresectable Advanced or Recurrent Solid Tumors

This study is to evaluate the tolerability and safety of ONO-7428 in participants with unresectable advanced or recurrent solid tumors.

Participants needed: 60
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Jan 12, 2026Locations: 15
Eligibility criteria

Participants with histologically or cytologically confirmed unresectable advance... [+4]

Participants with a complication or history of severe hypersensitivity to any ot... [+5]

Status: Recruiting

ONO-4059 Study in Patients With Steroid-resistant Pemphigus

ONO-4059-10:Multicenter, placebo-controlled, randomized, double-blind, Phase 3 study in patients with steroid-resistant pemphigus

Participants needed: 34
Trial details
Phase: Phase 3Age: 20+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Jan 7, 2026Locations: 25
Eligibility criteria

Patients with a diagnosis of pemphigus [+1]

Patients with an active infection [+2]

Status: Recruiting

ONO-2017 Study Japanese Patients With Primary Generalized Tonic Clonic Seizures.

To investigate the efficacy and safety of ONO-2017 in combination with antiepileptics in Japanese epileptic patients with generalized tonic-clonic seizures.

Participants needed: 15
Trial details
Phase: Phase 3Age: 12+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Jun 17, 2025Locations: 25
Eligibility criteria

Gender and age: Japanese patients, regardless of gender, aged 12 years or older... [+3]

Subject has a history of status epilepticus that required hospitalization within... [+4]

Status: Recruiting

Safety of Cenobamate in Japanese Subjects With Partial Onset Seizures

To evaluate the long-term safety and tolerability of cenobamate in Japanese epilepsy patients with partial seizures

Participants needed: 100
Trial details
Phase: Phase 2Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Jun 3, 2025Locations: 29
Eligibility criteria

Subjects completed Study YKP3089C035 by SK Life Science.

Subjects that have previously discontinued for any reason from the Core study (Y... [+1]

Status: Recruiting

A Phase I Study to Investigate the Tolerability and Safety of ONO-4685 Given as Monotherapy in T Cell Lymphoma and CLL/SLL

A Phase I Study to Investigate the Tolerability and Safety of ONO-4685 Given as Monotherapy in T Cell Lymphoma and CLL/SLL

Participants needed: 108
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Jun 3, 2025Locations: 14
Eligibility criteria

Angioimmunoblastic T-cell lymphoma(AITL) [+8]

Patients with severe complications. [+1]

Status: Recruiting

ONO-4538 Phase II Rollover Study (ONO-4538-98)

This study is intended to confirm the long-term safety of ONO-4538 in pan-tumor participants being treated with ONO-4538 monotherapy or in Combination with Other Therapies in clinical trials.

Participants needed: 59
Trial details
Phase: Phase 2Age: 16+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Jun 3, 2025Locations: 38
Eligibility criteria

Participant who is being treated with ONO-4538 as monotherapy or in Combination... [+1]

Participant judged to be incapable of providing consent for reasons such as conc... [+1]