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Extended clinical study of DSP-1958

Extended clinical study of DSP-1958

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080223598
Enrollment
100
Registered
2017-07-25
Start date
2017-09-19
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pediatric solid tumor, pediatric brain tumor, malignamt lymphoma

Interventions

Sponsors

Dainippon Sumitomo Pharma Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Collected adequate dose of hematopoietic stem cells. 2) Ability to understand and the willingness to sign a written informed consent form. 3) Negative pregnancy test. 4) Taking appropriate contraceptive measures. 5) ECOG PS of 0 to 2. 6) Adequate liver function, renal function, and cardiac function.

Exclusion criteria

Exclusion criteria: 1) Receiving any treatment for primary disease. 2) Received live attenuated vaccines within 90 days. 3) Pregnant or breastfeeding. 4) Uncontrolled intercurrent illness. 5) Patients who are receiving any other investigational agents. 6) Active infection. 7) History of allergic reaction attributed to compounds of similar chemical composition. 8) HIV Ab positive. 9) Planning or received within 14 days to treat hydropericardium, pleural effusion. 10) Patients who had grapefruits or grapefruits juice, or St. John's wort within 13 days. 11) Unsuitable for the clinical trial 12) Unable to receive adequate rehydration and frequent blood transfusion. 13) Received hematopoietic transplantation within 6 months.

Design outcomes

Primary

MeasureTime frame
safety efficacy Safety Adverse Events, Adverse drug reactions

Secondary

MeasureTime frame
efficacy other Efficacy(Other) 100-day survival rate, engrafment

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026