Clinical trials

20

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

Condition / disease
Location
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: Oct 9, 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-4538HSC in Pediatric Patients With Malignant Solid Tumors and in Patients With Epithelioid Sarcoma.

This is a multicenter, open-label, uncontrolled Phase I/II study to evaluate the efficacy, safety, and pharmacokinetics of ONO-4538HSC in pediatric patients with malignant solid tumors and in patients with epithelioid sarcoma, and to evaluate the tolerability in pediatric patients. The objective of this study is to explore the tolerability, safety, efficacy, and pharmacokinetics of ONO-4538HSC in patients with pediatric malignant solid tumors. The other objective is to exploratively investigate the efficacy and safety of ONO-4538HSC in patients with epithelioid sarcoma.

Participants needed: 50
Trial details
Phase: Phase 1, Phase 2Age: 12+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Oct 6, 2026Locations: 15
Eligibility criteria

Patients aged ≥ 12 to < 18 years at the time of signing the informed consent for... [+11]

Patients with current or previous severe hypersensitivity reactions to antibody... [+4]

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: Oct 5, 2026Locations: 17
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: Oct 1, 2026Locations: 36
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 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: Sep 25, 2026Locations: 39
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: Not yet recruiting

A Study of DCC-3014 to Evaluate the Efficacy, Safety, and Pharmacokinetics in Subjects With TGCT

To evaluate the efficacy, safety, and pharmacokinetics of DCC-3014 in subjects with Tenosynovial Giant Cell Tumor

Participants needed: 18
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Sep 22, 2026Locations: 1
Eligibility criteria

Histologically confirmed diagnosis of TGCT (tumor biopsy to confirm diagnosis wi... [+3]

Metastatic TGCT or other active malignancy that requires treatment, or history o... [+3]

Status: Not yet recruiting

A Trial of ONO-2808 in Participants With the Parkinsonian Subtype of Multiple System Atrophy (MSA-P)

The main goal of this clinical trial is to learn if ONO-2808 works to treat adults with the Parkinsonian subtype of Multiple System Atrophy (MSA-P). Researchers will compare ONO-2808 to a placebo (a look-alike substance that contains no drug) to see if ONO-2808 works to treat MSA-P. Participants will: * Take ONO-2808 or placebo orally for up to 48 weeks * Make visits to the clinic for checkups and tests * Answer questions about their health throughout the trial.

Participants needed: 486
Trial details
Phase: Phase 3Age: 30-80Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Sep 17, 2026
Eligibility criteria

Participants with a diagnosis of clinically established or clinically probable M... [+8]

Participants with the cerebellar subtype of MSA according to the 2022 MDS criter... [+5]

Status: Not yet recruiting

ONO-4915 in Patients With Primary Sjogren's Disease

To evaluate the efficacy and safety of ONO-4915 in patients with primary Sjogren's disease

Participants needed: 60
Trial details
Phase: Phase 2Age: 18-74Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Sep 16, 2026
Eligibility criteria

Age (at the time of informed consent): >=18 and <75 years [+5]

Patients with other concurrent autoimmune diseases [+6]

Status: Not yet recruiting

A Trial of ONO-4578 Versus Placebo in Combination With Nivolumab and Chemotherapy in Participants With Gastric Cancer, Esophagogastric Junction Cancer, or Esophageal Adenocarcinoma

The purpose of this study is to evaluate the efficacy and safety of ONO-4578 in combination nivolumab and chemotherapy in participants with advanced or metastatic gastric cancer, esophagogastric junction cancer, or esophageal adenocarcinoma. Participants will: * Receive either ONO-4578 with nivolumab and chemotherapy or placebo with nivolumab and chemotherapy. * Make visits to the clinic for checkups and tests. * Answer questions about their health throughout the trial.

Participants needed: 600
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Sep 14, 2026
Eligibility criteria

Have advanced or metastatic gastric cancer, esophagogastric junction cancer, or... [+5]

Participants with Human epidermal growth factor 2 (HER2)-positive or indetermina... [+4]

Status: Recruiting

A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of ONO-6414 Administered Orally in Healthy Adult Participants and Patients With Active Ulcerative Colitis

A study to investigate the safety, tolerability, and pharmacokinetics (PK) of ONO-6414 orally in healthy adult participants and in patients with active ulcerative colitis (UC).

Participants needed: 90
Trial details
Phase: Phase 1Age: 18-55Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Sep 9, 2026Locations: 1
Eligibility criteria

Male or female, age ≥18- to ≤55-year-old at the time of signing ICF. [+8]

Mentally or legally incapacitated. [+47]

Status: Recruiting

A Study of ONO-7429 in Participants With Unresectable Advanced or Recurrent Solid Tumors

This study is to evaluate the tolerability and safety of ONO-7429 in participants with unresectable advanced or recurrent solid tumors.

Participants needed: 80
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Ono Pharmaceutical Co., Ltd.Updated: Aug 26, 2026Locations: 10
Eligibility criteria

Participants with histologically or cytologically confirmed unresectable advance... [+3]

Participants with a history or presence of severe hypersensitivity to any other... [+5]

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: Aug 4, 2026Locations: 14
Eligibility criteria

Gender: Not specified [+3]

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

Status: 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: Jul 20, 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 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: Jul 16, 2026Locations: 39
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: 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

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

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

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]