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ONO-7913 Phase I Study (ONO-7913)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT04403308
Recruitment Status : Active, not recruiting
First Posted : May 27, 2020
Last Update Posted : May 10, 2021
Information provided by (Responsible Party):
Ono Pharmaceutical Co. Ltd

Brief Summary:
To assess the tolerability, safety, and pharmacokinetics (PK) of ONO-7913 in patients with advanced or metastatic solid cancers and explore its efficacy and biomarkers.

Condition or disease Intervention/treatment Phase
Solid Tumor Biological: ONO-7913 Phase 1

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 7 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: An Open-label, Uncontrolled, Dose Escalation Study in Patients With Advanced or Metastatic Solid Cancers (ONO-7913-01)
Actual Study Start Date : July 28, 2020
Estimated Primary Completion Date : May 2023
Estimated Study Completion Date : May 2023

Arm Intervention/treatment
Experimental: ONO-7913 as a Single Agent Biological: ONO-7913
ONO-7913 will be administered by intravenous continuous infusion during the designated time.

Primary Outcome Measures :
  1. Dose-limiting toxicities [ Time Frame: 28 days ]
    Number of participants with a DLT

  2. Adverse events [ Time Frame: Up to 24 months ]
    Assessed by the NCI CTCAE v5.0 criteria

Secondary Outcome Measures :
  1. Concentration vs time of ONO-7913 as single dose [ Time Frame: Up to 24 months ]
    PK profile

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   20 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  1. Patients with histologically or cytologically confirmed advanced or metastatic solid tumors
  2. ECOG Performance Status of 0-1
  3. Patients with life expectancy of at least 3 months

Exclusion Criteria:

  1. Patients with multiple cancers
  2. Patients with history of serious allergy

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT04403308

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Local Institution
Chuo-ku, Tokyo, Japan
Sponsors and Collaborators
Ono Pharmaceutical Co. Ltd
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Study Chair: Kazuhiro Nakabayashi Ono Pharmaceutical Co. Ltd
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Responsible Party: Ono Pharmaceutical Co. Ltd Identifier: NCT04403308    
Other Study ID Numbers: ONO-7913-01
First Posted: May 27, 2020    Key Record Dates
Last Update Posted: May 10, 2021
Last Verified: October 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No