Trametinib Combined With Everolimus and Lenvatinib for Recurrent/Refractory Advanced Solid Tumors

NCT ID: NCT04803318

Last Updated: 2024-06-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE2

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-01-01

Study Completion Date

2037-01-01

Brief Summary

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To study the clinical effect of Trametinib combined with Everolimus and Lenvatinib in the treatment of Recurrent/Refractory advanced solid tumors.

Detailed Description

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The tumor diameter was measured and the efficacy was evaluated after treatment with Trametinib combined with Everolimus and Lenvatinib.

Conditions

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Solid Tumor, Adult Hepatocellular Carcinoma

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

To treat recurrent or refractory advanced solid tumors with multiple targeting drugs that inhibit several critical signaling pathways in cancer cells.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Combination treatment of 3 inhibitors

Oral administration of 3 signaling pathways inhibitors: Mek inhibitor Trametinib, mTOR inhibitor Everolimus, and angiogenesis inhibitor Lenvatinib on refractory advanced solid tumors.

Group Type EXPERIMENTAL

Combination of three inhibitors Trametinib, Everolimus and Lenvatinib

Intervention Type DRUG

Oral administration of three inhibitors including Trametinib, Everolimus and Lenvatinib.

Interventions

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Combination of three inhibitors Trametinib, Everolimus and Lenvatinib

Oral administration of three inhibitors including Trametinib, Everolimus and Lenvatinib.

Intervention Type DRUG

Other Intervention Names

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Combination of 3 signaling pathway inhibitors specific to MEK, mTOR, and angiogenesis.

Eligibility Criteria

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Inclusion Criteria

* Recurrent/Refractory advanced solid tumors
* Age between 18 and 85 years
* Expected life expectancy is greater than three months

Exclusion Criteria

* Benign tumor
* Life expectancy is less than three months
* Serious medical commodities
* others
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Second Affiliated Hospital of Guangzhou Medical University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Zhenfeng Zhang, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Second Affiliated Hospital of Guangzhou Medical University

Locations

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The Second Affiliated Hospital of Guangzhou Medical University

Guangzhou, Guangdong, China

Site Status RECRUITING

Countries

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China

Central Contacts

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Zhenfeng Zhang, MD, PhD

Role: CONTACT

+862039195966

Bingjia He, MD

Role: CONTACT

+862039195966

Facility Contacts

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Zhenfeng Zhang, MD,PhD

Role: primary

+86-020-39195966

Bingjia He, MD

Role: backup

+86-14748877800

Other Identifiers

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ZZ3TKI-011

Identifier Type: -

Identifier Source: org_study_id

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