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NCT05925920COMPLETEDanonymous

A First in Human, Single Center, Single Dose, Randomized, Placebo-controlled, Dose, Escalating Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Subcutaneously Administered ENT-03S for the Treatment of Obesity and Diabetes

Sponsor

Source record

Metabolics Pharma

Phase

Source record

Phase 1

Modality

AI-normalized

small molecule

Target

AI-normalized

Not specified in the provided data; further investigation required to determine the precise molecular or mechanistic target profile of ENT-03S.

Indication / condition

AI-normalized

Obesity

Intervention

Source record

ENT-03, Placebo

Source & freshness

Source record

NCT ID

NCT05925920

Original source

ClinicalTrials.gov

Source last updated

Jun 01, 2026

Ingested at

Jun 13, 2026

Internal sync

Jun 13, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
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NCT ID

NCT05925920

Title

A First in Human, Single Center, Single Dose, Randomized, Placebo-controlled, Dose, Escalating Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Subcutaneously Administered ENT-03S for the Treatment of Obesity and Diabetes

Sponsor

Metabolics Pharma

Status

COMPLETED

Phase

Phase 1

Condition raw

Obesity, Diabetes Mellitus, Type 2

Condition normalized

Obesity, Diabetes Mellitus, Type 2

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Not specified in the provided data; further investigation required to determine the precise molecular or mechanistic target profile of ENT-03S.

Target normalized

Not specified in the provided data; further investigation required to determine the precise molecular or mechanistic target profile of ENT-03S.

Interventions

ENT-03, Placebo

Public preview

Source record

Metabolics Pharma's ENT-03S is positioned to address significant unmet needs in the obesity and Type 2 diabetes markets, which are characterized by a growing prevalence and limited effective treatment options. The trial's design, focusing on safety, tolerability, pharmacokinetics, and pharmacodynamics, suggests a strategic approach to mitigate risks associated with early-stage development. The competitive landscape includes established players with existing therapies, necessitating a robust differentiation strategy for ENT-03S. Successful outcomes could enhance Metabolics Pharma's market positioning and attract potential partnerships or acquisition interest, particularly if the drug demonstrates favorable efficacy and safety profiles.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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