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Other Disclosures4882Perseus Proteomics Inc.Pharmaceuticals

PPMX-T003: Results of clinical research involving participants in a Phase I clinical trial for polycythemia vera

In clinical research involving 6 patients who received PPMX-T003 in the Phase I trial for polycythemia vera, 4 patients were confirmed to have remained phlebotomy-free for at least 17 months after completing treatment.

Worth reading
65In focus
0–100. This measures how worthwhile something is to read, not how good or bad the company is.
Direction
Improvement
Direction inferred from the company’s description.
Scale
4
4 of 6 patients (phlebotomy-free for at least 17 months after completing treatment)
Wording
Conditional
How definitive the wording is.

Announced details

PPMX-T003 (the drug, T003)
Applicable field (uses covered by this announcement)

Polycythemia vera

What the company reported numerically
Quantitative Effects

Among the 6 patients who received PPMX-T003, 4 were confirmed to have remained phlebotomy-free for at least 17 months after completing treatment

Usage history

6 patients who received PPMX-T003 in the Phase I clinical trial

Relationship between the counterparty and the company
Perseus Proteomics Inc.4882
Relationship with the Company

The principal investigator and medical institution for clinical research involving participants in the Phase I clinical trial conducted by the Company

CounterpartyKansai Medical University Hospital

Department of Hematology and Oncology; principal investigator: Professor Ito Kazuki (伊藤量基)

Registration number and expiry date

Clinical research plan number: jRCT1050250129

Impact on Business Performance

There is no impact on the earnings forecast for the current fiscal year. The research is expected to contribute to an increase in corporate value over the medium to long term through future business development and other initiatives.

The company does not address Contract Value / Offering price.

Source (materials cited by the company)

Clinical Research Plan Submission and Disclosure System (jRCT)

Announced details
ItemDetails
Names of Products / Services CoveredPPMX-T003 (the drug, T003)
CounterpartyKansai Medical University Hospital
Counterparty overviewDepartment of Hematology and Oncology; principal investigator: Professor Ito Kazuki (伊藤量基)
Relationship with the CompanyThe principal investigator and medical institution for clinical research involving participants in the Phase I clinical trial conducted by the Company
Applicable areaPolycythemia vera
Registration number and expiry dateClinical research plan number: jRCT1050250129
Quantitative EffectsAmong the 6 patients who received PPMX-T003, 4 were confirmed to have remained phlebotomy-free for at least 17 months after completing treatment
Usage history6 patients who received PPMX-T003 in the Phase I clinical trial
Impact on Business PerformanceThere is no impact on the earnings forecast for the current fiscal year. The research is expected to contribute to an increase in corporate value over the medium to long term through future business development and other initiatives.
SourceClinical Research Plan Submission and Disclosure System (jRCT)
Items this document does not state (8)
Contract ValueOffering priceContract DateLaunch dateAward/certification nameAwarding / certifying bodyLocationLocation scale

These are items the company does not state in this document. We do not leave them blank, nor fill them in from other sources or by inference.

The reasons the company gives

The company's own explanation, not something inferred from the numbers.

Clinical research was conducted involving participants in the Phase I clinical trial to explore trends in changes in disease status based on the pharmacodynamic effects of PPMX-T003 and changes in laboratory test values.

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PPMX-T003: Results of clinical research involving participants in a Phase I clinical trial for polycythemia vera | Perseus Proteomics Inc. (4882) timely disclosure | Komori