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Buspirone/zolmitriptan

pharmaceutical compound

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General referenceInterpretive dossier study · Crown Archives visual atlas
Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionJul 12, 2026
Entity authorityQ138023914
Source-derived summary

Buspirone/zolmitriptan, also known by its developmental code names AV-2860 and JM-010, is a combination of buspirone, a serotonin 5-HT1A receptor partial agonist, and zolmitriptan, a serotonin 5-HT1B, 5-HT1D, 5-HT1E, and 5-HT1F receptor agonist, which is under development for the treatment of drug-induced dyskinesia, specifically levodopa-induced dyskinesia in people with Parkinson's disease. It is taken orally. The drug is under development by Contera Pharma and Bukwang Pharmaceutical. As of November 2024, it is in phase 2 clinical trials for treatment of drug-induced dyskinesia. Buspirone/zolmitriptan has failed to meet its endpoints in phase 2 trials.

Editorial summary

Begin with the source’s own compact description: “Buspirone/zolmitriptan” is pharmaceutical compound. The dossier treats that line as a proposition to test through Buspirone, zolmitriptan and pharmaceutical, not as a finished interpretation.

Editorial reviewA practical starting point whose main value is the path it opens into stronger specialist and primary sources. The current lead gives the account dated anchors—2024—that can be checked directly. The selected authority fields contribute no independent date. For this dossier, Buspirone, zolmitriptan and pharmaceutical is the immediate research focus.
Editorial analysis

Why this record matters

The phrase “pharmaceutical compound” supplies a clear boundary for inquiry. It also exposes the unanswered questions: who defined that boundary, when it became stable and which sources sit outside it.

Evidence profile

Vocabulary and entity names are the principal evidence signals here, because they determine the precision of every later search. The source revision retrieved here is dated Jul 12, 2026. The linked authority identifier is Q138023914. None of the 0 selected statements returned an explicit reference. The first chronological checks are 2024.

Critical limits

Overview language is designed for orientation and should not be treated as a substitute for the evidence cited beneath it. The lead is largely declarative, so disagreement and counter-evidence require a deliberate search beyond the opening account. Authority statements aid reconciliation but still require their own references, qualifiers and ranks to be checked.

How to read it

Use the entry as an orientation point, then follow its citations and revision history. Names, dates and institutional relationships should be checked against the original record.

Best used for
  • Subject orientation
  • Search vocabulary
  • Locating named sources
Verify next

The closest primary source, responsible institution and strongest cited specialist reference.

Three-step research path

  1. Establish the record: confirm the title “Buspirone/zolmitriptan”, its source revision and the description used here.
  2. Expand the search: follow Buspirone/zolmitriptan primary sources, Buspirone/zolmitriptan archive and Buspirone research across catalogues and specialist indexes.
  3. Test the account: compare the strongest cited source with the responsible institution’s current record and note any disagreement.

Questions for further research

  1. Which source most directly establishes the central claim about “Buspirone/zolmitriptan”?
  2. Which institution is responsible for the underlying evidence?
  3. Which cited source is closest to the event, object or claim?
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Source & attribution

This entry incorporates text from Buspirone/zolmitriptan” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.