Komori
Other Disclosures190AChordia Therapeutics Inc.Pharmaceuticals

Notice Regarding the Presentation of Dose-Escalation Cohort Data for rogocekib at the 2026 European Hematology Association (EHA) Congress

For the ongoing Phase 1/2 trial of rogocekib (CTX-712) in the United States, safety and preliminary efficacy data from the dose-escalation cohort were presented at the EHA Congress in June 2026. Among 34 evaluable patients, 4 objective responses were confirmed, for an ORR of 11.8%.

Worth reading
61In 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
11.8
% (ORR, 4/34 patients)
Wording
Conditional
How definitive the wording is.

Announced details

rogocekib(CTX-712)
Applicable field (uses covered by this announcement)

Myeloid malignancies, including relapsed or refractory acute myeloid leukemia (AML) and high-risk myelodysplastic syndromes (MDS)

Launch date13 June 2026 (described as a poster presentation; whether it is scheduled or has already taken place is not specified)
What the company reported numerically
Quantitative Effects

ORR of 11.8% (4/34 patients), CRi in 3 patients with AML, mCR in 1 patient with MDS, and a reduction of 50% or more in bone marrow blasts in 5 of 14 patients with splicing mutations

Usage history

34 evaluable patients and 42 patients enrolled in the trial (23 with AML, 16 with MDS and 3 with CMML)

Relationship between the counterparty and the company
Chordia Therapeutics Inc.190A
Relationship with the Company

A forum for presenting data from clinical trials conducted by the Company. Capital, personnel and business relationships are not disclosed.

CounterpartyEuropean Hematology Association (EHA)

A professional association in the field of hematology. Other information, including its location, representative and business activities, is not disclosed.

Registration number and expiry date

NCT05732103 (clinical trial registration number); expiration date not disclosed

In this announcement the company addresses none of Contract Value / Offering price / Impact on Business Performance.

Source (materials cited by the company)

European Hematology Association (EHA) abstract No. EHA-3974; NCT05732103; Yokoyama H et al., Blood Advances 2026; 10(1): 262-272; Sato J et al., Clin Cancer Res. 2026; doi: 10.1158/1078-0432.CCR-25-4896

Announced details
ItemDetails
Names of Products / Services Coveredrogocekib(CTX-712)
CounterpartyEuropean Hematology Association (EHA)
Counterparty overviewA professional association in the field of hematology. Other information, including its location, representative and business activities, is not disclosed.
Relationship with the CompanyA forum for presenting data from clinical trials conducted by the Company. Capital, personnel and business relationships are not disclosed.
Launch date13 June 2026 (described as a poster presentation; whether it is scheduled or has already taken place is not specified)
Applicable areaMyeloid malignancies, including relapsed or refractory acute myeloid leukemia (AML) and high-risk myelodysplastic syndromes (MDS)
Registration number and expiry dateNCT05732103 (clinical trial registration number); expiration date not disclosed
Quantitative EffectsORR of 11.8% (4/34 patients), CRi in 3 patients with AML, mCR in 1 patient with MDS, and a reduction of 50% or more in bone marrow blasts in 5 of 14 patients with splicing mutations
Usage history34 evaluable patients and 42 patients enrolled in the trial (23 with AML, 16 with MDS and 3 with CMML)
SourceEuropean Hematology Association (EHA) abstract No. EHA-3974; NCT05732103; Yokoyama H et al., Blood Advances 2026; 10(1): 262-272; Sato J et al., Clin Cancer Res. 2026; doi: 10.1158/1078-0432.CCR-25-4896
Items this document does not state (8)
Contract ValueOffering priceContract DateAward/certification nameAwarding / certifying bodyLocationLocation scaleImpact on Business Performance

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.

Because rogocekib demonstrated antitumor activity as monotherapy and manageable safety even in a patient population of older adults with multiple prior lines of treatment and limited treatment options.

How to read this page

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Notice Regarding the Presentation of Dose-Escalation Cohort Data for rogocekib at the 2026 European Hematology Association (EHA) Congress | Chordia Therapeutics Inc. (190A) timely disclosure | Komori