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NCT06480760RECRUITINGanonymous

Effects of Carnosine In Patients With Peripheral Arterial Disease Patients; Randomized Intervention Trial (CIPHER)

Sponsor

Source record

Shahid Baba

Phase

Source record

Phase 1/2

Modality

AI-normalized

small molecule

Target

AI-normalized

Carnosine supplementation for improving walking ability in patients with Peripheral Arterial Disease (PAD).

Indication / condition

AI-normalized

Peripheral Arterial Disease

Intervention

Source record

Carnosine

Source & freshness

Source record

NCT ID

NCT06480760

Original source

ClinicalTrials.gov

Source last updated

May 29, 2025

Ingested at

Jun 18, 2026

Internal sync

Jun 18, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT06480760

Title

Effects of Carnosine In Patients With Peripheral Arterial Disease Patients; Randomized Intervention Trial (CIPHER)

Sponsor

Shahid Baba

Status

RECRUITING

Phase

Phase 1/2

Condition raw

Peripheral Arterial Disease

Condition normalized

Peripheral Arterial Disease

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Carnosine supplementation for improving walking ability in patients with Peripheral Arterial Disease (PAD).

Target normalized

Carnosine supplementation for improving walking ability in patients with Peripheral Arterial Disease (PAD).

Interventions

Carnosine

Public preview

Source record

The CIPHER trial, sponsored by Shahid Baba at the University of Louisville, is investigating the efficacy of carnosine supplementation in enhancing walking ability among patients with PAD. Given the prevalence of PAD and the limited treatment options available, a successful outcome could position carnosine as a novel therapeutic intervention in this space. The market for PAD treatments is significant, with increasing demand for effective management strategies. Competitive analysis indicates that while there are existing pharmacological treatments, none specifically target the metabolic pathways influenced by carnosine. This trial could provide a unique selling proposition if successful, potentially leading to partnerships or licensing opportunities with larger pharmaceutical companies. Diligence should focus on the safety profile of carnosine and its regulatory pathway, as well as the potential for market exclusivity based on trial outcomes.

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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