- First stated window
- “in late 2026 / early 2027”SEC Exhibit 99.1, filed
- Disclosure date
- None foundLast checked:
Timeline
How wording is compared
Equivalent half-year, quarter, and year notations are compared together while original wording stays visible. Qualifiers such as early, mid, late, and end remain distinct. A slash and or are compared together for two complete timing alternatives with explicit years. Each source is compared with the preceding checked date. Different wording in documents from the same day is shown separately, without assigning an order within that day. No comparison is made against a preceding date with different timing expressions. Status is set by founder review of the original filings.
| Document | Date | Event retained | Exact company wording | Review | Source |
|---|---|---|---|---|---|
| SEC Exhibit 99.1 | Initial entry within checked sources: “in late 2026 / early 2027” | Anticipate topline data in late 2026 / early 2027 | Checked by founder | SEC original | |
| SEC Exhibit 99.1 | Statement retained: “in late 2026 or early 2027” | Septerna anticipates reporting data from the trial in late 2026 or early 2027. | Checked by founder | SEC original | |
| SEC Form 10-Q | Statement retained: “late 2026 or early 2027” | We anticipate reporting data from the trial in late 2026 or early 2027. | Checked by founder | SEC original | |
| Company press release | Wording changed: “late 2026 or early 2027” → “in the first quarter of 2027”Sources (2) | As a result, Septerna expects to report Phase 1 data from both the SAD and MAD cohorts in the first quarter of 2027. | Checked by founder | Company original | |
| SEC Form 10-Q | Wording changed: “late 2026 or early 2027” → “in the first quarter of 2027”Sources (2) | As a result, we expect to report Phase 1 data from both the SAD and MAD cohorts in the first quarter of 2027. | Checked by founder | SEC original | |
| SEC Form 10-Q | Context disclosed | To fully characterize steady-state pharmacokinetics, dosing for the MAD cohorts will be extended to 14 days. Part I, Item 2: Recent Developments, SEP-479 PTH1R Agonist Program; paragraph beginning Based on pharmacokinetic data (page 23) | Checked by founder | SEC original |
Sources
- SEC Exhibit 99.1 — filed 2026-01-12
- SEC Exhibit 99.1 — filed 2026-04-13
- SEC Form 10-Q — filed 2026-05-11
- Company press release — company release 2026-08-10
- SEC Form 10-Q — filed 2026-08-10
- Company release — 2026-08-10
- Company release — 2026-09-10
- Company press release listing — checked 2026-10-10
- Context: SEC Form 10-Q — filed 2026-08-10 · Part I, Item 2: Recent Developments, SEP-479 PTH1R Agonist Program; paragraph beginning Based on pharmacokinetic data (page 23)
Last checked: . Compared by hand with the original filings by Jiwoo Seong (Woo).
Corrections
| Date | What changed | Why | Evidence |
|---|---|---|---|
| Corrected the April 13 event label to Statement retained; removed that equivalent expression from Wording changes. | The comparison treats late 2026 / early 2027 and late 2026 or early 2027 as equivalent timing alternatives. Original quotations are retained. | January 12 SEC Exhibit 99.1 and April 13 SEC Exhibit 99.1, retained in First stated and Changes. | |
| Added the August 10 10-Q sentence about extending MAD cohort dosing to 14 days as a Context disclosed row. | Founder requested the exact company quotation and original filing link. | https://www.sec.gov/Archives/edgar/data/1984086/000119312526342353/sepn-20260630.htm | |
| Updated the Changes explanation to: Status is set by founder review of the original filings. | The status is the founder-selected status retained in the reviewed record. | Founder correction request on 2026-10-10; the reviewed Timing changed status is retained. |
A correction is added here with its date, what changed, why, and the evidence. The earlier version is not deleted. Report an error: hello@orionbiotechai.com. If you want your name shown with the correction, include it; otherwise no name is shown.
