Clinical Pipeline

Cagrilintide

NN9833

Cagrilintide is a clinical-stage asset. Trial status and sponsor-reported findings remain time-sensitive and indication-specific.

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EvidenceTier 2
RegulatoryInvestigational
SafetyKnown but Manageable Risks
Clinical phasePhase 3
01

Overview

ClassLong-acting amylin analogue
Sponsor / developerNovo Nordisk
Review statusReviewed
Record IDPEP-020
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Plain-language guide

What it was designed or studied for

Designed for research into Obesity, Type 2 diabetes. It remains investigational for these uses.

How it works, simply

It copies or works with amylin, a hormone signal involved in fullness and how quickly food leaves the stomach.

This simplified explanation is educational context, not a treatment recommendation or a substitute for the clinical evidence below.
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Clinical mechanism

Activates amylin receptors and is being studied alone and with semaglutide.

Mechanism plausibility is not the same as demonstrated clinical benefit.
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Applications

  • Obesity
  • Type 2 diabetes
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Human evidence

Early or mid-stage human data exist, but confirmation, replication or long-term follow-up remains incomplete.

Tier 2
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Preclinical evidence

Mechanistic and preclinical findings are tracked separately and are not treated as proof of human clinical benefit.

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Regulatory status

Investigational. Regulatory status is product- and jurisdiction-specific and does not automatically follow from an evidence score.

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Safety

Known but Manageable Risks

  • Adverse effects vary by product and indication
  • Contraindications and interactions require label review
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Interactions

Review the current product label and indication-specific literature for pharmacologic and absorption interactions.

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Treatment pattern

Treatment patterns are product-, indication- and clinician-specific; this educational profile does not provide dosing guidance.

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Manufacturing and quality

Approved-product identity, formulation and quality controls must not be extrapolated to compounded or RUO copies.

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Sources

  1. 01
    Primary regulatory record

    Source record prepared for primary-reference linking in the Supabase-backed editorial workflow.

  2. 02
    Clinical trial registry

    Source record prepared for primary-reference linking in the Supabase-backed editorial workflow.

  3. 03
    Peer-reviewed literature

    Source record prepared for primary-reference linking in the Supabase-backed editorial workflow.

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Gaps and unverified claims

  • Long-term outcomes and real-world safety are not yet established.
  • Current phase and catalysts require primary-source confirmation.
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Last reviewed

August 5, 2026 · Reviewed