Search hospitals

>

Texas

>

Houston

Texas Children's Hospital

Claim this profile

Houston, Texas 77030

Global Leader in Brain Tumor

Global Leader in Cancer

Conducts research for HIV Infection

Conducts research for Leukemia

Conducts research for Mixed-Cell Lymphoma

782 reported clinical trials

118 medical researchers

Photo of Texas Children's Hospital in HoustonPhoto of Texas Children's Hospital in Houston

Summary

Texas Children's Hospital is a medical facility located in Houston, Texas. This center is recognized for care of Brain Tumor, Cancer, HIV Infection, Leukemia, Mixed-Cell Lymphoma and other specialties. Texas Children's Hospital is involved with conducting 782 clinical trials across 1,168 conditions. There are 118 research doctors associated with this hospital, such as Jennifer Foster, MD, Patricia Baxter, MD, Carlos Ramos, MD, and Rayne H. Rouce.

Area of expertise

1

Brain Tumor

Global Leader

Texas Children's Hospital has run 50 trials for Brain Tumor. Some of their research focus areas include:

BRAF positive
H3.3K27M positive
Stage IV
2

Cancer

Global Leader

Texas Children's Hospital has run 40 trials for Cancer. Some of their research focus areas include:

Stage IV
CD70 positive
EWSR1-FLI1 translocation positive

Top PIs

Clinical Trials running at Texas Children's Hospital

Cancer

Crohn's Disease

Brain Tumor

Adrenoleukodystrophy

Inflammatory Bowel Disease

Cystic Fibrosis

Type 2 Diabetes

Leukoencephalopathy

Genetic Disorders

Craniopharyngioma

Image of trial facility.

Onivyde + Talazoparib/Temozolomide

for Ewing Sarcoma

The phase I portion of this study is designed for children or adolescents and young adults (AYA) with a diagnosis of a solid tumor that has recurred (come back after treatment) or is refractory (never completely went away). The trial will test 2 combinations of therapy and participants will be randomly assigned to either Arm A or Arm B. The purpose of the phase I study is to determine the highest tolerable doses of the combinations of treatment given in each Arm. In Arm A, children and AYAs with recurrent or refractory solid tumors will receive 2 medications called Onivyde and talazoparib. Onivyde works by damaging the DNA of the cancer cell and talazoparib works by blocking the repair of the DNA once the cancer cell is damaged. By damaging the tumor DNA and blocking the repair, the cancer cells may die. In Arm B, children and AYAs with recurrent or refractory solid tumors will receive 2 medications called Onivyde and temozolomide. Both of these medications work by damaging the DNA of the cancer call which may cause the tumor(s) to die. Once the highest doses are reached in Arm A and Arm B, then "expansion Arms" will open. An expansion arm treats more children and AYAs with recurrent or refractory solid tumors at the highest doses achieved in the phase I study. The goal of the expansion arms is to see if the tumors go away in children and AYAs with recurrent or refractory solid tumors. There will be 3 "expansion Arms". In Arm A1, children and AYAs with recurrent or refractory solid tumors (excluding Ewing sarcoma) will receive Onivyde and talazoparib. In Arm A2, children and AYAs with recurrent or refractory solid tumors, whose tumors have a problem with repairing DNA (identified by their doctor), will receive Onivyde and talazoparib. In Arm B1, children and AYAs with recurrent or refractory solid tumors (excluding Ewing sarcoma) will receive Onivyde and temozolomide. Once the highest doses of medications used in Arm A and Arm B are determined, then a phase II study will open for children or young adults with Ewing sarcoma that has recurred or is refractory following treatment received after the initial diagnosis. The trial will test the same 2 combinations of therapy in Arm A and Arm B. In the phase II, a participant with Ewing sarcoma will be randomly assigned to receive the treatment given on either Arm A or Arm B.

Recruiting

1 award

Phase 1 & 2

14 criteria

Image of trial facility.

Tagraxofusp

for Blood Cancers

Tagraxofusp is a protein-drug conjugate consisting of a diphtheria toxin redirected to target CD123 has been approved for treatment in pediatric and adult patients with blastic plasmacytoid dendritic cell neoplasm (BPDCN). This trial aims to examine the safety of this novel agent in pediatric patients with relapsed/refractory hematologic malignancies. The mechanism by which tagraxofusp kills cells is distinct from that of conventional chemotherapy. Tagraxofusp directly targets CD123 that is present on tumor cells, but is expressed at lower or levels or absent on normal hematopoietic stem cells. Tagraxofusp also utilizes a payload that is not cell cycle dependent, making it effective against both highly proliferative tumor cells and also quiescent tumor cells. The rationale for clinical development of tagraxofusp for pediatric patients with hematologic malignancies is based on the ubiquitous and high expression of CD123 on many of these diseases, as well as the highly potent preclinical activity and robust clinical responsiveness in adults observed to date. This trial includes two parts: a monotherapy phase and a combination chemotherapy phase. This design will provide further monotherapy safety data and confirm the FDA approved pediatric dose, as well as provide safety data when combined with chemotherapy. The goal of this study is to improve survival rates in children and young adults with relapsed hematological malignancies, determine the recommended phase 2 dose (RP2D) of tagraxofusp given alone and in combination with chemotherapy, as well as to describe the toxicities, pharmacokinetics, and pharmacodynamic properties of tagraxofusp in pediatric patients. About 54 children and young adults will participate in this study. Patients with Down syndrome will be included in part 1 of the study.

Recruiting

1 award

Phase 1

Image of trial facility.

Long-Term Effects Study

for Childhood Cancer Survivors

The Childhood Cancer Survivor Study (CCSS) will investigate the long-term effects of cancer and its associated therapies. A retrospective cohort study will be conducted through a multi-institutional collaboration, which will involve the identification and active follow-up of a cohort of approximately 50,000 survivors of cancer, diagnosed before 21 years of age, between 1970 and 1999 and 10,000 sibling controls. This project will study children and young adults exposed to specific therapeutic modalities, including radiation, chemotherapy, and/or surgery, who are at increased risk of late-occurring adverse health outcomes. A group of sibling controls will be identified and data collected for comparison purposes.

Recruiting

1 award

N/A

3 criteria

Similar Hospitals nearby

Frequently asked questions

What kind of research happens at Texas Children's Hospital?

Where is Texas Children's Hospital located?

Who should I call to ask about financial aid or insurance network?

What insurance does Texas Children's Hospital accept?

What awards or recognition has Texas Children's Hospital received?

Unbiased Results

We believe in providing patients with all the options.

Your Data Stays Your Data

We only share your information with the clinical trials you're trying to access.

Verified Trials Only

All of our trials are run by licensed doctors, researchers, and healthcare companies.

Terms of Service·Privacy Policy·Cookies·Security

Unbiased Results

We believe in providing patients with all the options.

Your Data Stays Your Data

We only share your information with the clinical trials you're trying to access.

Verified Trials Only

All of our trials are run by licensed doctors, researchers, and healthcare companies.

Terms of Service·Privacy Policy·Cookies·Security