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NCT05608876ACTIVE_NOT_RECRUITINGanonymous

A Phase II, Open Label, Single Arm Study To Assess The Efficacy Of Intratumoral Tigilanol Tiglate In Various Head And Neck Solid Malignancies

Sponsor

Source record

QBiotics Group Limited

Phase

Source record

Phase 2

Modality

AI-normalized

small molecule

Target

AI-normalized

Tigilanol tiglate targets tumor cells through a mechanism that induces necrosis and apoptosis, potentially enhancing local immune response against tumors.

Indication / condition

AI-normalized

Head and Neck Cancer

Intervention

Source record

Tigilanol Tiglate

Source & freshness

Source record

NCT ID

NCT05608876

Original source

ClinicalTrials.gov

Source last updated

Aug 07, 2025

Ingested at

Jun 13, 2026

Internal sync

Jun 13, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT05608876

Title

A Phase II, Open Label, Single Arm Study To Assess The Efficacy Of Intratumoral Tigilanol Tiglate In Various Head And Neck Solid Malignancies

Sponsor

QBiotics Group Limited

Status

ACTIVE_NOT_RECRUITING

Phase

Phase 2

Condition raw

Head and Neck Cancer

Condition normalized

Head and Neck Cancer

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Tigilanol tiglate targets tumor cells through a mechanism that induces necrosis and apoptosis, potentially enhancing local immune response against tumors.

Target normalized

Tigilanol tiglate targets tumor cells through a mechanism that induces necrosis and apoptosis, potentially enhancing local immune response against tumors.

Interventions

Tigilanol Tiglate

Public preview

Source record

QBiotics Group Limited is advancing tigilanol tiglate in a Phase II clinical trial for various head and neck solid malignancies. The market for head and neck cancer therapies is significant, with a growing demand for innovative treatments due to the limitations of existing therapies. The trial's open-label, single-arm design suggests a focused approach to assess efficacy and safety, which could position tigilanol tiglate as a novel intratumoral treatment option. However, the competitive landscape includes established therapies and emerging immunotherapies, necessitating robust clinical data to demonstrate superior efficacy or safety profiles. Diligence should focus on patient recruitment, trial execution, and the potential for regulatory hurdles given the investigational nature of the drug.

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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