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Eikon Therapeutics (EIKN) pipeline and stated timing

Pipeline at a glance

ProgramEventStageStated timingFiling
EIK1001/data readoutStage not statedin October 202610-Q ·
EIK1003Topline/data readoutStage not statedin October 202610-Q ·
EIK1003Topline/data readoutStage not statedin October 202610-Q ·
EIK1005Topline/data readoutStage not statedin October 202610-Q ·
EIK1003Topline/data readoutStage not statedESMO Congress 2026 in October10-Q ·
EIK1004Topline/data readoutStage not statedESMO Congress 2026 in October10-Q ·
EIK1006 submission—by the end of 202610-Q ·

Source: ORION, orionbiotechai.com/company/EIKN, data as of Oct 16, 2026
https://www.orionbiotechai.com/company/EIKN

Nearest upcoming stated timing: EIK1001 · Topline/data readout · in October 2026

SEC sources last checked .

Programs and stated timing

○ Quote matched to filing (not yet reviewed by founder) · ✓ Checked by founder.

Topline/data readoutin October 2026

Stage: Not stated

Public float: Unknown (no public float found in SEC filings).

We expect to present updated data from TeLuRide-005 at the 2026 European Society of Medical Oncology, or ESMO, Congress in October 2026.

SEC timing context:

We completed enrollment in TeLuRide-005 in the first quarter of 2026.

10-Q · Filed · Last checked

Source details

Accession 0001193125-26-349185

SEC accepted the filing

Topline/data readoutin October 2026

Stage: Not stated

Public float: Unknown (no public float found in SEC filings).

We plan to present updated data from Cohort 1A at the ESMO Congress 2026 in October 2026.

SEC timing context:

We are evaluating EIK1003 in Cohort 1A as a monotherapy for the treatment of patients with ovarian, breast, prostate, and pancreatic cancers.

10-Q · Filed · Last checked

Source details

Accession 0001193125-26-349185

SEC accepted the filing

Topline/data readoutin October 2026

Stage: Not stated

Public float: Unknown (no public float found in SEC filings).

We plan to present the updated clinical data from Cohort 1C at the ESMO Congress 2026 in October 2026.

SEC timing context:

Cohort 1C is evaluating EIK1003 in combination with paclitaxel for the treatment of patients with platinum-resistant ovarian cancer or patients with HER2-negative breast cancer that have failed hormonal therapy if ER+ or chemotherapy if ER negative.

10-Q · Filed · Last checked

Source details

Accession 0001193125-26-349185

SEC accepted the filing

Topline/data readoutin October 2026

Stage: Not stated

Public float: Unknown (no public float found in SEC filings).

We plan to present initial clinical data from this trial at the ESMO Congress 2026 in October 2026.

SEC timing context:

We are currently evaluating EIK1005 in a Phase 1/2 trial as monotherapy and in 25 combination with pembrolizumab in participants with advanced solid tumors.

10-Q · Filed · Last checked

Source details

Accession 0001193125-26-349185

SEC accepted the filing

Topline/data readoutESMO Congress 2026 in October

Stage: Not stated

Public float: Unknown (no public float found in SEC filings).

We plan to present initial clinical data from Cohort 1B at the ESMO Congress 2026 in October.

SEC timing context:

Cohort 1B is evaluating EIK1003 in combination with abiraterone and prednisone for the treatment of patients with advanced prostate cancer.

10-Q · Filed · Last checked

Source details

Accession 0001193125-26-349185

SEC accepted the filing

Topline/data readoutESMO Congress 2026 in October

Stage: Not stated

Public float: Unknown (no public float found in SEC filings).

We plan to present the first clinical data from this trial at the ESMO Congress 2026 in October.

SEC timing context:

We are also conducting a Phase 1/2 trial evaluating the safety and efficacy of EIK1004, our selective PARP1 inhibitor designed to penetrate the central nervous system, for the treatment of patients with ovarian, breast, prostate, and pancreatic cancers.

10-Q · Filed · Last checked

Source details

Accession 0001193125-26-349185

SEC accepted the filing

NDA/BLA submissionby the end of 2026

Stage: —

Public float: Unknown (no public float found in SEC filings).

We expect to submit an investigational new drug application, or IND, for EIK1006 by the end of 2026.

10-Q · Filed · Last checked

Source details

Accession 0001193125-26-349185

SEC accepted the filing

How this date was described over time

Company periods and sentences are quoted as written. A matching disclosure uses the SEC filing date for the same program and event type. As of .

Program / eventStated period and SEC wordingDisclosure in stated period
EIK1001Clinical resultsin October 2026
“We expect to present updated data from TeLuRide-005 at the 2026 European Society of Medical Oncology, or ESMO, Congress in October 2026.”

Filed · 10-Q

Still within period

As of Oct 19, 2026

EIK1003Clinical resultsin October 2026
“We plan to present updated data from Cohort 1A at the ESMO Congress 2026 in October 2026.”

Filed · 10-Q

Still within period

As of Oct 19, 2026

EIK1003Clinical resultsESMO Congress 2026 in October
“We plan to present initial clinical data from Cohort 1B at the ESMO Congress 2026 in October.”

Filed · 10-Q

Not compared

ORION has no confirmed start and end dates for this wording, so it is not compared with filings.

EIK1003Clinical resultsin October 2026
“We plan to present the updated clinical data from Cohort 1C at the ESMO Congress 2026 in October 2026.”

Filed · 10-Q

Still within period

As of Oct 19, 2026

EIK1004Clinical resultsESMO Congress 2026 in October
“We plan to present the first clinical data from this trial at the ESMO Congress 2026 in October.”

Filed · 10-Q

Not compared

ORION has no confirmed start and end dates for this wording, so it is not compared with filings.

EIK1005Clinical resultsin October 2026
“We plan to present initial clinical data from this trial at the ESMO Congress 2026 in October 2026.”

Filed · 10-Q

Still within period

As of Oct 19, 2026

EIK1006Submissionby the end of 2026
“We expect to submit an investigational new drug application, or IND, for EIK1006 by the end of 2026.”

Filed · 10-Q

Not compared

ORION has no confirmed start and end dates for this wording, so it is not compared with filings.

“Not compared” means ORION has not matched this wording against a complete set of SEC filings for its period. It says nothing either way about whether a matching filing exists. Wording without exact dates is not given calendar dates.

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Reading these records

First stated window
The timing wording in the earliest company statement located within the sources checked, quoted as written (for example “2H 2026”). An earlier statement may exist outside those sources.
Disclosure date
The date of the filing or company release that disclosed the readout. “None found” means no such disclosure was located in the sources checked. SEC filings were searched through the “SEC filings searched through” date shown.
1H, 2H, 1Q–4Q
First or second half, or first to fourth quarter, of the year named, as the company wrote it. Equivalent notations are compared together; the original wording stays visible.
SEC original
The filing as published on the SEC EDGAR system. “Company original” is the release on the company's own investor site.
Status
One of seven labels set by founder review of the original filings. Definitions: Methodology.

See EIKN in the calendar · Review labels and methodology

Topline results are the main summary results of a clinical trial, released before the full data.A New Drug Application (NDA) or Biologics License Application (BLA) asks the FDA to approve a drug or biologic for sale.