Has Eli Lilly publicly disclosed trial identifiers, press releases, or peer‑reviewed data for a drug named Neurocept reported to have Phase II Alzheimer’s results?

Checked on January 9, 2026
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Executive summary

There is no evidence in the provided reporting that Eli Lilly has publicly disclosed trial identifiers, press releases, or peer‑reviewed data for any drug called "Neurocept"; the company has, however, widely disclosed such materials for donanemab — a distinct investigational antibody whose Phase 2 and Phase 3 programs were reported in press releases and peer‑reviewed journals [1] [2] [3] [4]. The reporting suggests "Neurocept" does not appear in the documents supplied, so any claim that Eli Lilly publicly disclosed information about a Phase II Alzheimer’s result for a drug by that name is unsupported by these sources.

1. The question being asked and what the sources actually cover

The user’s query asks a straightforward provenance question — has Eli Lilly publicly posted identifiers, press materials, or peer‑reviewed papers for a drug named Neurocept with Phase II Alzheimer’s results — but the supplied reporting centers on donanemab (formerly LY3002813/N3pG), not a molecule called Neurocept [5] [1]. None of the provided items mention "Neurocept," so the dataset does not substantiate public disclosures by Lilly under that name [2] [3].

2. What Eli Lilly has publicly disclosed — the donanemab record

Eli Lilly has repeatedly issued press releases and investor statements about donanemab’s clinical program, including Phase 2 topline and full data releases and later Phase 3 results; company investor news items announce Phase 2 results and the larger TRAILBLAZER‑ALZ 2 Phase 3 outcomes [1] [2] [4] [6]. The Phase 2 proof‑of‑concept trial was published in the New England Journal of Medicine and explicitly lists the ClinicalTrials.gov identifier TRAILBLAZER‑ALZ (NCT03367403), while TRAILBLAZER‑ALZ 2 (Phase 3) is registered as NCT04437511 and is described in Lilly materials [3] [4].

3. Peer‑reviewed publications and independent commentary

Peer‑reviewed data for donanemab are present in high‑profile journals: the Phase 2 TRAILBLAZER‑ALZ trial was published in NEJM and later Phase 3 data were published or presented in JAMA and at major Alzheimer conferences, with the National Institute on Aging and independent outlets reporting on those papers [3] [4] [7]. Scientific outlets such as Science and AAAS covered the fuller donanemab dataset and highlighted requests from outside scientists for more granular safety and subgroup data, signaling that while core peer‑reviewed material exists, independent observers still seek additional disclosure on risk factors and subgroup analyses [8] [9].

4. Press releases, SEC filings, and corporate framing

Lilly has used investor news releases and PR channels to announce trial results — a normal practice reinforced by regulatory and market disclosure rules noted in reporting (for example, Lilly’s news release required by the SEC when announcing Phase 3 results) — and those releases are cited across the sources [10] [11]. That corporate framing comes with implicit motives: companies use press releases to shape investor and regulator expectations, and some reports note potential conflicts of interest among authors and consultants, which readers should weigh when interpreting company‑sponsored analyses [3] [10].

5. Direct answer to the question, limits of the reporting, and plausible explanations

Based on the provided reporting, Eli Lilly has not publicly disclosed trial identifiers, press releases, or peer‑reviewed data for any drug named "Neurocept" — there are no citations or documents here that link Lilly to that name; instead the reporting documents substantial public disclosure for donanemab, including ClinicalTrials.gov identifiers (NCT03367403 and NCT04437511), company press releases, and peer‑reviewed NEJM/JAMA publications for donanemab [3] [4] [1] [2]. If "Neurocept" is an alternate or trade name, that fact is not supported by these sources; the supplied materials identify donanemab (LY3002813/N3pG) as the molecule with Phase 2/Phase 3 Alzheimer’s results and do not equate it to "Neurocept" [5] [3]. The reporting therefore answers decisively given the available evidence: no documented Lilly disclosures for "Neurocept" appear here, while abundant disclosures exist for donanemab.

Want to dive deeper?
Is 'Neurocept' a registered drug name or trademark, and does it correspond to any public clinical trial records?
How do donanemab's trial identifiers (NCT03367403, NCT04437511) map to published NEJM/JAMA papers and conference presentations?
What additional subgroup and safety data have external scientists requested about donanemab, and where can those datasets be accessed?