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NNC6022-0004

Phase 1

Obesity | Small molecule | Immunology |Novo Nordisk A/S|Last Updated: Sep 1, 2026

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLED
Total Trials1
Total Enrollment128

FDA Designations

No designations recorded

Clinical trial landscape

NNC6022-0004 · 1 trial · 2 indications

Phase 1 1
NCT07693868A Study to See How Safe a New Medicine (NNC6022-0004) is in Healthy People and People Living With ObesityObesity
RECRUITING128 Analytics
PHASE1RECRUITING
A Study to See How Safe a New Medicine (NNC6022-0004) is in Healthy People and People Living With Obesity
ObesityUnlock trial analytics

Study Endpoints

Primary Endpoints

Part A: Area under the NNC6022-0001 plasma concentration-time curve from time 0 to last measurable plasma concentration (AUC0-tz) after a single dose
From pre-dose (Day 1) until visit 3 (Day 9)

Measured as micromolar per hour (µM\*h).

Part A: Maximum observed plasma concentration (Cmax) of NNC6022-0001 after a single dose
From pre-dose (Day 1) until visit 3 (Day 9)

Measured as micromolar (µM).

Part B: Number of treatment emergent adverse events (TEAE)
From time of dosing (Day 1) to end of study visit (Day 14)

Measured as number of events.

Part C: Number of treatment emergent adverse events
From time of dosing (Day 1) to end of study visit (Day 41)

Measured as number of events.

Part D: Area under the NNC6022-0001 plasma concentration-time curve from time 0 to last measurable plasma concentration (AUC0-tz) after a single dose
From pre-dose (Day 1 or Day 8) to end of visit (Day 5 or Day 12)

Measured as µM\*h.

Part E: Number of treatment emergent adverse events
From time of dosing (Day 1) to end of study visit (Day 13)

Measured as number of events.

Secondary Endpoints

Part A: The area under the NNC6022-0001 plasma concentration-time curve from time 0 to infinity (AUC0-∞) after a single dose
From pre-dose (Day 1) until visit 3 (Day 9)
Part A: Number of treatment emergent adverse events
From time of dosing (Day 1) to end of study visit (Day 9)
Part B: The area under the NNC6022-0001 plasma concentration-time curve from time 0 to last measurable plasma concentration (AUC0-tz) after a single dose
From pre-dose (Day 1) until visit 3 (Day 9)
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Study Design & Arms

AllocationRANDOMIZED
MaskingQUADRUPLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
NNC6022-0004EXPERIMENTALParticipants will receive NNC6022-0004 administered orally as a single ascending dose (SAD), multiple ascending dose (MAD), or under fed/fasted conditions.
PlaceboPLACEBO_COMPARATORParticipants will receive placebo matched to NNC6022-0004 administered orally as a SAD, MAD, or under fed/fasted conditions.

Interventions

NameTypeDescription
NNC6022-0004DRUGParticipants will receive single dose of NNC6022-0004 administered orally in capsule form.
PlaceboDRUGParticipants will receive placebo matched to NNC6022-0004 administered orally in capsule form.
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Eligibility Criteria

Age Range18 Years to 65 Years
SexALL
Healthy VolunteersYes
Study Sites1

Inclusion Criteria: * Male, or female of non-childbearing potential. * For Parts A, B, C and D: Age 18-55 years (both inclusive) at the time of signing the informed consent. For optional Part E only: Age 18-65 years (both inclusive) at the time of signing the informed consent. -For Parts A, B, C ...

Countries:Netherlands
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Recent Changes (Last 90 Days)

LOWSep 1, 2026NCT07693868primaryCompletionDate: changed
LOWSep 1, 2026NCT07693868primaryCompletionDate: changed
LOWAug 20, 2026NCT07693868Status: NOT_YET_RECRUITING → RECRUITING
LOWAug 20, 2026NCT07693868Status: NOT_YET_RECRUITING → RECRUITING
LOWAug 20, 2026NCT07693868Status: NOT_YET_RECRUITING → RECRUITING
LOWAug 20, 2026NCT07693868Status: NOT_YET_RECRUITING → RECRUITING
LOWJul 9, 2026NCT07693868NEW_TRIAL: changed
LOWJul 9, 2026NCT07693868NEW_TRIAL: changed

Frequently asked questions about NNC6022-0004

What is NNC6022-0004 used for?

NNC6022-0004 is an investigational small molecule being developed for obesity. It is also being studied in people with elevated high-sensitivity C-reactive protein (hsCRP), a marker of inflammation. The drug is currently in Phase 1 clinical development and has not been approved by regulatory authorities.

Who is developing NNC6022-0004?

NNC6022-0004 is being developed by Novo Nordisk A/S, a biopharmaceutical company listed on the stock exchange under the ticker NVO. The company is conducting clinical trials to evaluate the safety and tolerability of this investigational drug in healthy volunteers and people living with obesity.

What phase is NNC6022-0004 in?

NNC6022-0004 is in Phase 1 clinical development. It is an investigational drug, meaning it has not been approved by regulatory authorities and is still being studied in clinical trials. The ongoing Phase 1 trial is recruiting participants to assess the drug's safety profile.

What clinical trials is NNC6022-0004 in?

NNC6022-0004 is being studied in a Phase 1 clinical trial registered as NCT07693868. This randomized, double-blind, placebo-controlled study is evaluating the safety of the drug in healthy people and people living with obesity. The trial is recruiting 128 participants in the Netherlands and is currently active.

Is NNC6022-0004 being studied in people with elevated hsCRP?

Yes, NNC6022-0004 is being studied in people with obesity and elevated high-sensitivity C-reactive protein (hsCRP). The ongoing Phase 1 trial includes participants with these conditions to evaluate how safe the drug is in this population. The study is recruiting healthy volunteers as well as people with obesity.