Houston, TXNCT01189786Now EnrollingIRB Ready

Stem Cell Transplant Clinical Trial in Houston, TX

Access cutting-edge stem cell transplant treatment through this clinical trial at a research site in Houston. Study-provided care at no cost to qualified participants.

Sponsored by Baylor College of Medicine

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Expert Care in Houston

Access stem cell transplant specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related stem cell transplant treatment provided free

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Check if you qualify for this stem cell transplant clinical trial in Houston, TX

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Why Participate?

  • No-Cost Study Care

  • Local to Houston

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Houston site if eligible
  4. 4Begin participation

About This Stem Cell Transplant Study in Houston

Participants are being asked to take part in this study because treatment of his or her disease requires a stem cell transplant. Stem cells or "mother" cells are the source of normal blood cells and lead to recovery of blood counts after bone marrow transplantation. Unfortunately, there is not a perfectly matched stem cell donor (like a sister or brother) for the participant and his or her disease does not permit enough time to identify another donor (like someone from a registry list that is not his or her relative) or another suitable donor has not been identified. However, a close relative of the patient has been identified whose stem cells are not a perfect match, but can be used. Alternatively, the patient may have already received a stem cell transplant but have evidence of mixed chimerism, which means some of the patient's own bone marrow cells are present, rather than all of the donor's cells. This may lead to an increased risk of the disease coming back. Or, the patient may have all donor cells but his or her bone marrow is not working very well, which may lead to frequent blood or platelet (cells that help in clotting blood) transfusions or infection. Regardless of the reason, it may be necessary to isolate stem cells from a haploidentical (half-match) donor in order to provide bone marrow function. Because the stem cells from the donor are only half-matched to the participant, the risk of graft-versus-host disease (GvHD) is very high. GvHD is a complication after transplant caused by donor T cells (graft) that attack the transplant recipient, and this complication can cause death after transplant. Thus, it is important that the donor's blood cells are treated to minimize cells that are most likely to attack the host's tissues. This is done by using a special device to capture the CD34+ stem cells from the donor's stem cell product prior to giving the cells to the host. This method minimizes the donor T cells, which are responsible for causing GvHD. Purpose: In an effort to lower the occurrences and severity of graft-versus-host disease in patients and to lower the rate of transplant failure, investigators would like to specially treat the donor's blood cells to minimize the cells that are most likely to attack the patient's tissues.

Sponsor: Baylor College of Medicine

Who Can Participate

Inclusion Criteria

for Stem Cell Transplant WITH Conditioning (COHORT 1)
Patient requiring allogeneic SCT
Age between birth and 70 years
Patient and/or responsible person able to understand and sign consent

Exclusion Criteria

for Stem Cell Transplant WITH Conditioning (COHORT 1)
Active, acute GvHD \> grade II or extensive, chronic GvHD
Severe life, threatening infection
Pulmonary dysfunction (FEV1, FVC or DLCO 40% of predicted or 3 SD below normal)
Cardiac dysfunction (LVSF less than 25%)
Psychiatric disturbance
Lansky or Karnofsky score \< 50%
The presence of severe hepatic disease (direct bilirubin \>3x upper limit of normal and AST \> 5x upper limit of normal).
Creatinine \> 3x normal
Known HIV Positivity
Pregnancy Inclusion Criteria for CD34+ Topoff WITHOUT conditioning (COHORT 2)
Allogeneic SCT Recipient requiring additional cellular therapy
Age between birth and 70 years
Patient and/or responsible person able to understand and sign consent
At least ONE of the following must be answered YES for a patient to be eligible to receive CD34+ topoff:
Evidence of mixed chimerisms (less than 95% donor cells)
Evidence of poor bone marrow function (bone marrow cellularity less than 50% with at least one cytopenia)
Relapsed or persistent disease Exclusion criteria for CD34+ Topoff WITHOUT conditioning (COHORT 2)
Active, acute GvHD \> grade II or extensive, chronic GvHD
Severe life, threatening infection
Known HIV positivity
Pregnancy Inclusion Criteria for CD34+ Topoff WITH conditioning (COHORT 3)
Allogeneic SCT Recipient requiring additional cellular therapy
Age between birth and 70 years
Patient and/or responsible person able to understand and sign consent
At least ONE of the following must be answered YES for a patient to be eligible to receive CD34+ topoff:
Evidence of mixed chimerisms (less than 95% donor cells)
Evidence of poor bone marrow function (bone marrow cellularity less than 50% with at least one cytopenia)
Relapsed or persistent disease Exclusion criteria for CD34+ Topoff WITH Conditioning (COHORT 3)
Active, acute GVHD \> grade II or extensive, chronic GvHD
Severe life, threatening infection
Pulmonary disfunction (FEV1, FVC or DLCO 40% of predicted or 3 SD below normal)
Cardiac dysfunction (LVSF less than 25%)
Psychiatric disturbance
Lansky or Karnofsky score \< 50%
The presence of severe hepatic disease (direct bilirubin \> 3x upper limit of normal and AST \> 5x upper limit of normal)
Creatinine \> 3x normal
Known HIV positivity

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Houston?

Yes, this clinical trial (NCT01189786) has an active research site in Houston, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Stem Cell Transplant Treatment Options in Houston, TX

If you're searching for stem cell transplant treatment options in Houston, TX, this clinical trial (NCT01189786) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Houston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced stem cell transplant specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all stem cell transplant clinical trials near you to find additional studies recruiting in your area.

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