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NCT07172126NOT_YET_RECRUITINGanonymous

A Phase I/II Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of TQB3201 Tablets in Patients With Advanced Prostate Cancer

Sponsor

Source record

Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

Phase

Source record

Phase 1/2

Modality

AI-normalized

small molecule

Target

AI-normalized

Androgen Receptor (AR) and E3 ligase (CRBN)

Indication / condition

AI-normalized

Metastatic Castration-resistant Prostate Cancer

Intervention

Source record

TQB3201 tablets

Source & freshness

Source record

NCT ID

NCT07172126

Original source

ClinicalTrials.gov

Source last updated

Sep 15, 2025

Ingested at

May 19, 2026

Internal sync

May 23, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT07172126

Title

A Phase I/II Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of TQB3201 Tablets in Patients With Advanced Prostate Cancer

Sponsor

Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

Status

NOT_YET_RECRUITING

Phase

Phase 1/2

Condition raw

Metastatic Castration-resistant Prostate Cancer

Condition normalized

Metastatic Castration-resistant Prostate Cancer

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Androgen Receptor (AR) and E3 ligase (CRBN)

Target normalized

Androgen Receptor (AR) and E3 ligase (CRBN)

Interventions

TQB3201 tablets

Public preview

Source record

TQB3201, a PROTAC drug targeting the Androgen Receptor (AR), is positioned to address unmet needs in advanced prostate cancer treatment, particularly in patients resistant to current therapies like abiraterone and enzalutamide. The market for advanced prostate cancer therapies is expanding, with increasing demand for innovative treatments that can overcome resistance mechanisms. Given the competitive landscape, TQB3201's unique mechanism of action may provide a significant advantage, potentially leading to a strong market position if clinical efficacy is demonstrated. Diligence should focus on the competitive landscape, particularly other emerging therapies targeting AR and the potential for partnerships or licensing agreements to enhance market entry and distribution.

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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