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South Texas Accelerated Research Therapeutics

San Antonio, TX, US
New

South Texas Accelerated Research Therapeutics (START) directs clinical trials of novel anticancer agents using a high quality and innovative information technology infrastructure to ensure accurate and rapid clinical trials in a setting that emphasizes personalized and compassionate clinical care. START’s head office is located in San Antonio, Texas, in the heart of the South Texas Medical Center.

With centers located in the US, Spain and China START conducts the world’s largest Phase I medical oncology program – putting more than 400 patients per year on Phase I trials. Patients travel from all over the world to participate in one or more of our Phase I drug trials.

START consists of a team of highly trained physicians and staff with extensive experience in Phase I clinical trials research and are nationally recognized as thought leaders in cancer research and drug development.

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Phase I clinical trials
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At START, we provide quality data through timely enrollment of study participants. The Phase I Clinic staff is comprised of a variety of specialized team members including Registered Nurses, Licensed Vocational Nurses, Front Desk Schedulers, Research Nurses, Study Coordinators, Clinical Research Assistants, and Medical Records... Show more »

At START, we provide quality data through timely enrollment of study participants. The Phase I Clinic staff is comprised of a variety of specialized team members including Registered Nurses, Licensed Vocational Nurses, Front Desk Schedulers, Research Nurses, Study Coordinators, Clinical Research Assistants, and Medical Records Technicians all dedicated entirely to the Phase I program. Staff members are trained in Good Clinical Practices (GCP) and are also highly experienced in the field of oncology. Certifications held within the department include Oncology Certified Nurse (OCN), Advanced Cardiac Life Support (ACLS), Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), and Registered Health Information Technician (RHIT).

The Director of Phase I Nursing, Leslie Smetzer, holds a Bachelor of Science degree in Nursing, is an Oncology Certified Nurse and has over 25 years of oncology as well as 20 years in Phase I clinical trial experience.

Exam

The exam area at START includes 10 exam rooms for our clinical trial participants. Using state-of the-art wireless technology and a physician data capture system, our highly trained physicians are able to assess patients at bedside to document, grade, attribute adverse events, and enter the data digitally into our electronic medical record (EMR). This permits accurate assessment at point of contact.

Treatment

The START clinic has a research dedicated treatment room for clinical trial patients. This area includes 21 treatment chairs and 3 bed/gurney areas. The treatment staff consists of Registered Nurses who provide direct patient care and include OCN and ACLS certified RNs. They provide IV infusions and oral medications as well as obtain pharmacokinetic, pharmacodynamic and other specimens required during treatment and observation periods.

The START clinic has uninterrupted digital cardiac monitoring capabilities in early and late development clinical studies. At START we utilize a wireless Holter monitoring system for cardiac and QTc evaluations.

Research Nurses / Study Coordinators

The Research Staff consists of Research Nurses and Study Coordinators who are responsible for protocol management, communication with study sponsors, and patient care. Our research staff is responsive to both patient and study sponsor needs. Each study is assigned a research team member to ensure continuity of care for study patients as well as the needs of the study sponsor. The research staff is closely involved with patient screening, enrollment, education, and patient follow up. They maintain constant communication with study sponsors, physicians, clinical staff, and patients.

Data Management

START’s data management team consists of experienced Clinical Research Assistants (CRAs) that are responsible for paper and electronic case report form (CRF) completion, and query resolution. The team is highly knowledgeable with electronic data capture (EDC) systems, such as, Medidata Rave, InForm, Oracle Clinical, and Synteract. The CRAs are also responsible for coordinating all aspects of monitoring visits at START. The team is held to the upmost internal standards to ensure a quality and timely product for the study sponsors. Our data management team undergoes quality and timeliness assessment with the study sponsor at every exit interview to ensure quality standards are maintained.

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Preclinical Efficacy Studies
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Biomarker Discovery
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Orthotopic Tumor Animal Models
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Maximum Tolerated Dose (MTD) Studies
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Drug Discovery & Development
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Drug Discovery & Development Services

Drug Discovery & Development Services

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Animal Models and Studies
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Animal Models and Studies Services

Animal Models and Studies Services

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Oncology Animal Models
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Oncology Animal Models Services

Oncology Animal Models Services

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Clinical Research
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Clinical Research Services

Clinical Research Services

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Animal Models of Disease
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Animal Models of Disease Services

Animal Models of Disease Services

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Clinical Trials, Consulting, and Management
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Clinical Trials, Consulting, and Management Services

Clinical Trials, Consulting, and Management Services

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Pharmacology & Toxicology
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Pharmacology & Toxicology Services

Pharmacology & Toxicology Services

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Bioanalysis
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Bioanalysis Services

Bioanalysis Services

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Biomarkers
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Biomarkers Services

Biomarkers Services

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ADME and DMPK Studies
Drug Metabolism and Pharmacokinetics
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ADME and DMPK Studies Services

ADME and DMPK Studies Services

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