Tag: Drug Development

Southern Research teams investigate Zika virus and its damaging mechanisms

Aedes aegypti mosquito
The Zika virus is carried by the Aedes Aegypti mosquito.

Scientists at Southern Research are heavily involved in the global fight against Zika, and are examining five different strains of the virus in a broad-based effort to penetrate the mysteries of a virus that was seen as posing little threat before being linked to devastating neurological abnormalities in unborn children as well as other maladies.

Through this multi-pronged inquiry, infectious disease experts in the Drug Discovery and Drug Development divisions at Southern Research have engaged in basic and applied science to better understand Zika, while exploring how the mosquito-borne virus progresses in infected human neural cells. Scientists are also using these virus stocks to develop in vivo models to evaluate potential vaccines and treatments.

In March, Southern Research developed the first in vitro antiviral assay for the Zika virus, giving researchers and drug developers worldwide a testing platform for new compounds and biologics capable of interfering with Zika virus infection and replication by detecting the accumulation of progeny virus in cull culture supernatants.

Timothy Sellati, Ph.D., chair of the Department of Infectious Diseases in Southern Research’s Drug Discovery division, said the Zika investigation aims to reveal the mechanisms that cause microcephaly, a rare disorder that causes a baby’s brain and head to be abnormally small.

“If we can understand how this virus affects normal human RNA, we may be able to develop therapeutics that can either eradicate the virus entirely or at least neutralize the virus’ ability to cause such severe damage to normal brain development,” Sellati said.

SUDDEN THREAT

Jonathan Rayner, director of Infectious Disease Research
Jonathan Rayner, director of Infectious Disease Research

After a surge in microcephaly cases in Brazil, the U.S. Centers for Disease Control in April confirmed the link between the birth defect and Zika. The virus has also been recently associated with Guillain-Barré Syndrome, a rare condition causing muscle weakness and temporary paralysis, as well as other illnesses in pediatric and adult populations.

“The more we learn about Zika, the more we realize how complex this virus truly is,” said Jonathan Rayner, Ph.D., Southern Research’s director of Infectious Disease Research. “While in the past, Zika was understood to be arthropod-borne virus associated with limited clinical pathology, we are now seeing increased transmission by previously unrecognized routes, including sexual transmission, and it is becoming increasingly associated with significant maladies in both newborns and adults.”

The virus was first identified in Uganda’s Zika Forest in 1947. Since this time, there have been several other outbreaks in various equatorial regions of the world, but Zika’s sudden emergence as a public-health hazard in the Americas makes developing a complete understanding of the virus a critical priority, Rayner said.

As part of that effort, Southern Research’s infectious disease researchers are studying five unique strains of the virus, each isolated in the geographic locations of a previous outbreak.

“One interesting question is whether, over this span of time, the Zika virus changed genetically in terms of its virulence and its ability to cause disease, particularly neurological diseases like microcephaly or Guillain-Barré Syndrome,” Sellati said.

“That’s a question we’re able to address in-house here at Southern Research.”

COORDINATED EFFORT

Southern Research is well positioned to take a leading role in the fight against Zika. With fully developed labs dedicated to drug discovery and drug development, the organization has deep experience in infectious disease research, including mosquito-borne viruses, and a longstanding history of exploring new drugs for a wide range of cancers and other maladies.

“We have a lot of experience working with other viruses in the same family as Zika,” Rayner said. “Dengue is a very good example. We have very active drug-screening programs against dengue and have developed the associated in vivo models to support drug development. West Nile virus is another example, as is Japanese encephalitis, yellow fever – we’ve established research programs and models for all of those.”

Tim Sellati, chair of Infectious Diseases, Drug Discovery.
Tim Sellati, chair of the Department of Infectious Diseases.

Sellati said teams of experts from various fields at Southern Research are collaborating on the Zika investigation, with the common goal of gaining insights that can combat the virus’ harmful spread.

“When you see the tiny brains, the tiny skulls of these children born with microcephaly, it’s amazing how devastating this viral infection on the normal development of the cerebral cortex,” he said. “We hope our research will help the scientific community better understand the aggressive nature of this virus, as we work collectively to fight its spread and develop effective therapeutic approaches.”

The Developmental and Reproductive Toxicology (DART) program at Southern Research is poised to assist Sellati and Rayner as a partner in this effort. Researchers in the organization’s DART program have decades of experience and expertise, which will be invaluable assets in the program to determine how Zika is able to interrupt normal brain development.

“Once we have a better understanding of the complex interactions between the Zika-infected mother and child, we can help define a strategy to effectively prevent or mitigate Zika-induced birth defects,” said Paul Bushdid, DART program leader.

Southern Research appoints Paul Bushdid to direct DART program

Paul Bushdid, Ph.D., Developmental & Reproductive Toxicology Program Leader
Paul Bushdid, Ph.D., Developmental & Reproductive Toxicology Program Leader

BIRMINGHAM, Ala. – April 7, 2016 – Paul Bushdid, Ph.D., has joined Southern Research to lead its Developmental & Reproductive Toxicology (DART) program, which performs complex preclinical studies to ensure that potential medicines, nutraceuticals and environmental chemicals don’t endanger unborn children and pregnant women, and don’t negatively affect fertility in men and women.

Bushdid brings extensive experience as a study director and investigative team leader to the Birmingham-based institute, which is involved in a critical research program to evaluate the long-term health effects of chemical exposures early in life.

Prior to joining Southern Research this month, Bushdid worked for 13 years at global pharmaceutical company GlaxoSmithKline, where he headed an Investigative Developmental Toxicology group. In this role, he managed a team of study directors and technical scientists focusing on teratogens, or agents that can cause birth defects or halt pregnancies.

At GlaxoSmithKline, Bushdid’s team was also involved in DART assessments of traditional Chinese medicines, study designs needed for cell and gene therapy products, and data requirements for the use of nanomaterials in non-clinical development.

“I am excited and ready to act as a resource for the growth and development of the DART program at Southern Research,” Bushdid said. “Our goal is simple but important – protect the children.”

CRITICAL MISSION

Southern Research’s DART program provides a full range of safety evaluation services and Good Laboratory Practice-compliant assessments that determine a chemical’s effects on fertility, fetal development and post-natal outcomes.

In 2013, Southern Research was awarded a contract from the National Institute of Environmental Health Sciences to study the potential impact on early-life exposure to certain chemicals, and to determine their effects on development and reproductive systems. The contract has a potential value of $70 million over 10 years.

“The reproductive toxicology studies we perform at Southern Research are necessary to ensure new materials do not pose a health hazard to unborn children and mothers,” said Art Tipton, Ph.D., president and CEO. “We are thrilled Paul is bringing his expertise and leadership abilities to SR to direct the critical mission of our DART program.”

Bushdid received a Ph.D. in microbiology and immunology from the Vanderbilt University School of Medicine in 2000 and served as a post-doctoral fellow at the Cincinnati Children’s Hospital Medical Center before joining GlaxoSmithKline in 2003.

About Southern Research
Southern Research is a not-for-profit 501(c)(3) organization with more than 400 scientists and engineers working across four divisions: drug discovery, drug development, engineering, and energy and environment. We work on behalf of the National Cancer Institute, National Institutes of Health, the U.S. Department of Defense, the U.S. Department of Energy, NASA, major aerospace firms, utility companies, and other private and government organizations as we solve the world’s hardest problems. SR, founded in 1941, is headquartered in Birmingham with additional laboratories and offices in Wilsonville and Huntsville, Alabama; Frederick, Maryland; Durham, North Carolina; Cartersville, Georgia; and Houston.

E.A. Dulmadge: Pursuing a research dream and attacking cancer

Elizabeth Ann Dulmadge – E.A., as she was known to her friends — arrived at Southern Research Institute in 1956 with more than a decade of experience in a clinical microbiology laboratory. She soon became involved in a significant new area of inquiry for the institute: cancer research.

Over several decades, Dulmadge’s work in Southern Research’s anticancer drug screening program helped the Birmingham-based organization make important strides in the battle against a disease doctors still struggle to understand.

To mark Women’s History Month, Southern Research is highlighting the careers of some of the female scientists and technicians who have made meaningful contributions to the institute over its 75 years of scientific investigation.

“E.A. Dulmadge should be an inspiration to many young people today, particularly girls interested in science,” said Art Tipton, Ph.D., president and CEO of Southern Research. “E.A. pursued her dream of conducting research that could help save lives, and her valuable work over many years accomplished that.”

Dulmadge came to the institute after earning a bachelor’s degree in biology from Birmingham-Southern College and working for 11 years as supervisor of the clinical microbiology lab at University Hospital, now UAB.

“I wanted more of a challenge to see what I could do,” she recalled in a 1981 interview to mark her 25th anniversary at Southern Research.

CELL CULTURE WORK

Her sense of timing in 1956 was ideal. After arriving at Southern Research, she spent six months testing antiviral agents for pharmaceutical company Parke-Davis, then transferred to the institute’s fledgling anticancer drug screening program.

She worked alongside Dr. Frank Schabel, whose groundbreaking research with Dr. Howard Skipper and others at Southern Research advanced the role of chemotherapy as an effective cancer treatment and expanded the understanding of how to better counter the disease.

“Dr. Schabel put me in charge of the cell culture work since my background in microbiology was an excellent prerequisite for this type of work,” she recalled.

In those days, pharmaceutical companies were developing large numbers of synthetic drugs, and it was up to Southern Research to test them for the National Cancer Institute. Dulmadge and the team annually screened 5,000 to 7,000 compounds in cell cultures – cells grown under controlled conditions, perfect for experimental studies.

Over the years, she continued her work with cell cultures, investigating the effects of antitumor agents on laboratory-grown tumors and studying cells resistant to anticancer agents. Her inquiries included an extensive look into tumor stem cells, or those cells that give rise to cancer. She also developed effective methods of growing tumor colonies for the screening tests.

ANTICANCER ADVANCES

Dulmadge, who contributed to at least two dozen scientific papers with her Southern Research colleagues, felt a deep sense of accomplishment in the institute’s chemotherapy research.

“I think of how much more we know about cancer chemotherapy now that we did in the beginning of the program,” she said in the 1981 interview. “It’s been a privilege to work here.”

Dulmadge retired in 1992, after 36 years at Southern Research. At her death, she left a majority of her estate to Birmingham-Southern, which created the Elizabeth A. Dulmadge Scholarship Fund in 2004 for students majoring in biology or music.

Southern Research’s anticancer drug expertise has led to the discovery of six FDA-approved medicines that treat the disease. The organization remains a key player in cancer research, having received more than $90 million in funding from the National Institutes of Health over the past two decades.

Mary Trader: Unraveling leukemia’s mysteries in a Southern Research lab

Mary Trader
Mary Trader

When Mary Trader joined Southern Research in 1966, she had a bachelor’s degree in chemistry from St. Mary’s Dominican College in her hometown of New Orleans and plans to stick around for one year.

Trader’s one year blossomed into a long career at Southern Research that saw her rise to head the Experimental Leukemia Section, where she played a significant role in the institute’s pioneering chemotherapy work.

“You can’t help but feel you have made some contribution to eradicating a dread disease,” Trader recalled in a 1981 interview marking her 25th year at Southern Research.

Because March is Women’s History Month, Southern Research is highlighting the contributions of several of the organization’s prominent female scientists over its 75 years of operation.

“Southern Research has been fortunate to have employed many great women scientists like Mary Trader in its history,” said Art Tipton, Ph.D., president and CEO. “Their careful and thoughtful work in our labs has deepened the scientific community’s understanding of cancer and other diseases.”

Trader’s career at Southern Research began as the search for new cancer-fighting drugs accelerated in its Birmingham labs, thanks to a steady stream of funding from the National Cancer Institute. For Trader, the first few years were spent in a crowded lab in the Ingalls West building.

“At the beginning of the screening program, there was already a backlog of drugs that had never been tested against cancer,” she recalled. “We had a field day testing everything the government had to send us.”

IN THE LAB

In 1973, Trader was appointed head of the Experimental Leukemia Section. Her lab conducted work in mouse leukemia that contributed to improved cancer treatments, particularly of acute lymphocytic leukemia, or ALL.

In those days, ALL spread rapidly and often fatally in children, but because of advances coming from Southern Research and other organizations, survival rates began to rise sharply.

The work performed by Trader’s team contributed to these advances in several ways. For one thing, her lab developed at least 20 lines of drug-resistant leukemias that proved useful in testing drug treatments. These resistant forms of leukemia were utilized in biochemistry and cell culture studies to expose the mechanism of drug resistance.

“We want to know why a drug does not work in a person’s body and what happens to it,” Trader said in 1980.

In addition, extensive testing carried out in Trader’s lab demonstrated the validity of famed Southern Research cancer researcher Dr. Howard Skipper’s theory that just one cancer cell can trigger the fatal disease. Skipper introduced the concept that every single cancer cell must be eliminated to ensure the survival of the patient.

“This added some basic knowledge to understanding the magnitude of the disease of cancer,” Trader recalled.

Her lab also conducted studies on combination chemotherapy that explored how new and existing drugs could be used together or in sequence as an effective treatment regimen for leukemia and many different forms of cancer.

“Everything we have learned — proper scheduling of drugs, problems of drug resistance and demonstration of one cancer cell’s impact — has tied in with increasingly successful treatment of children with leukemia,” Trader said in 1980.

‘INSTANT RECALL’

Soon after marking 30 years at Southern Research, Trader died from a heart attack in 1987. She was 64 years old.

Dr. Russell Laster, then head of the institute’s Cancer Screening Division, noted her immense contribution to the organization’s work. “She was like a computer with 30 years of storage and instant recall, and you can’t replace that.”

During her career as an experimental cancer chemotherapist, Trader contributed to at least 30 scientific papers, including several with Skipper and another prominent figure in cancer research, Dr. Frank Schabel. She also presented her leukemia findings at national meetings held by the American Association for Cancer Research and others.

Southern Research scientists develop an assay to find a cure for Zika

Aedes aegypti mosquito
Aedes aegypti mosquito

BIRMINGHAM, Ala. – As reports of the Zika virus outbreak began to emerge from Brazil and portions of South and Central America, infectious disease researchers in the Drug Discovery labs of Southern Research were already taking steps to help combat its spread.

Today, Southern Research is proud to announce the development of a unique antiviral assay – a test that can be used by researchers worldwide to detect the virus in infected cell cultures. The assay is immediately available to meet the requirements of international clients. In addition, teams of experienced scientists at Southern Research are working to develop in vivo models that can be used to evaluate vaccines and therapeutic approaches aimed at preventing the further spread of Zika virus disease.

“Southern Research is uniquely positioned to support the efforts of the global scientific community as we work collectively to better understand, and ultimately stop the spread of this disease,” said Dr. Jonathan Rayner, Director of Infectious Disease Research at Southern Research in Birmingham. “With such a wide variety of skills and backgrounds under our roof, this team is comprised of experts from a number of different fields, including drug discovery, mosquito-borne infectious disease research, and biomedical engineering. This assay represents a crucial step in the global search for a vaccine, and we’re proud to be able to contribute to the growing body of science in this impactful way.”

Zika is a mosquito-borne virus that is thought to cause birth defects such as microcephaly in newborn children, if transmitted to women during the early stages of pregnancy. Earlier this year, the World Health Organization declared the spread of Zika a Public Health Emergency of international concern, and has since coordinated a global response. Southern Research has been able to support these efforts by leveraging their assay development and drug discovery experience.

Southern Research’s infectious disease research team focuses on a wide array of human infectious diseases including programs involved in the HIV Cure Initiative, Biodisease, Influenza clinical trial support, Dengue virus vaccine evaluations, Hepatitis and Poliovirus.

Drug development is deeply ingrained in the fabric of Southern Research. To date, research teams from the institute have discovered and developed seven cancer medications. Several of these drugs are currently being used by pediatric oncologists as an effective treatment in the fight against childhood cancer.

About Southern Research
Southern Research is a not-for-profit 501(c)(3) organization with more than 400 scientists and engineers working across four divisions: drug discovery, drug development, engineering, and energy and environment. We work on behalf of the National Cancer Institute, National Institutes of Health, the U.S. Department of Defense, the U.S. Department of Energy, NASA, major aerospace firms, utility companies, and other private and government organizations to solve the world’s hardest problems. Founded in 1941, Southern Research is headquartered in Birmingham with additional laboratories and offices in Wilsonville and Huntsville, Frederick, Maryland, Durham, North Carolina, Cartersville, Georgia, and Houston. Visit southernresearch.org for more information.

Southern Research Awarded New $22 Million NIAID-DAIDS Contract to Support Ground-Breaking HIV Cure Research

Red_Ribbon

BIRMINGHAM, Ala. – July 7, 2015 – Southern Research has been awarded a seven-year contract of up to $22 million to support research that could contribute to the cure of HIV disease. Under this contract, Southern Research will develop and standardize assays that quantitate latent reservoirs of HIV.

“This is a revolutionary area in HIV research that is opening up new avenues for us in infectious diseases,” said Southern Research President and CEO Art Tipton, Ph.D. “It supports our 24-year legacy in HIV drug discovery and development for government and pharmaceutical clients.”

HIV replication can be effectively suppressed in infected patients with antiretroviral therapy (ART), which reduces the level of HIV in the blood to an undetectable level. However, HIV remains a chronic infection due to its ability to stay hidden within these infected blood cells – latent reservoirs – that are invisible to the body’s immune defenses and are not sensitive to anti-HIV drugs. When a latently infected cell is reactivated the cell begins to produce HIV again.

In order to support the HIV cure initiative, Southern Research was awarded the National Institute of Allergy and Infectious Diseases (NIAID) contract HHSN272201500017C, “Quantitative Viral Outgrowth Assay (QVOA) Service Resource.” The QVOA is the current best assay for characterizing the latent viral reservoir. However, the assay is not available to many laboratories conducting HIV cure research because it is expensive and labor intensive. Southern Research will expand access to the QVOA and support future clinical research focused on eliminating the latent viral reservoir.

In addition to providing the QVOA as a service resource, Southern Research will work with experts in the field of HIV latency and cure research to develop alternative assays that are more sensitive, less costly, can be completed more rapidly, and require smaller amounts of blood than QVOA. Southern Research will also provide training in the performance of the QVOA to investigators interested in running the assay in their laboratories.

“Our team is excited and energized to be partnering with the HIV research community to enhance our collective understanding of the latent reservoirs of HIV in support of the HIV cure initiative,” said Southern Research Director, Infectious Disease Research and Principal Investigator for the contract Mike Murray, Ph.D.

Facts About HIV

  • Currently, there is no cure for AIDS caused by HIV, and the virus continues to spread despite the increased global commitment to controlling the pandemic.
  • HIV is the world’s leading infectious killer. According to the World Health Organization (WHO), an estimated 39 million people have died since the first cases were reported in 1981.
  • In 2013, globally, there were more than 35 million people living with HIV: 2.1 million people became newly infected and 1.5 million died.
  • In the U.S., there are more than 30 FDA approved HIV medicines. A variety of interventional agents are used in combination to control virus replication and successfully manage the disease, and they show promise in prevention of new infections.
  • Millions are relying on antiretroviral therapy (ART) until a sterilizing cure can be identified, but according to the latest Centers for Disease Control and Prevention’s Vital Signs report, only 3 in 10 people living with HIV have achieved viral suppression.
  • Oral administration of ART was approved worldwide to inhibit transmission in high risk populations and mother-to-child transmissions.
  • In 2013, approximately 12 million people received ART, but drug resistance is an ongoing issue.

About Southern Research
Southern Research is a not-for-profit 501(c)(3) organization with nearly 500 scientists and engineers working across four divisions: drug discovery, drug development, engineering, and energy and environment.

  • We’re developing 18 drugs to combat various forms of cancer, ALS, Alzheimer’s, diabetes, kidney disease, and Parkinson’s, among others.
  • We’ve developed seven FDA-approved cancer drugs.
  • We’re developing new medical devices.
  • We’re helping to launch manned missions to Mars.
  • We’re making the air and water cleaner here on Earth.

We work on behalf of the National Cancer Institute, National Institutes of Health, the U.S. Department of Defense, the U.S. Department of Energy, NASA, major aerospace firms, utility companies, and other private and government organizations as we solve the world’s hardest problems.

Southern Research, founded in 1941, is headquartered in Birmingham with additional laboratories and offices in Wilsonville and Huntsville, Frederick, Maryland, Durham, North Carolina, Cartersville, Georgia, and Houston. Visit SouthernResearch.org for more information.

 

How Drug Development Works

It can take 10 to 15 years for scientists to begin the journey of understanding a disease, to creating a drug that fights it.

  • IND Application: File Investigational New Drug application with the FDA before clinical testing.
  • Phase 1Clinical Trial: Perform human testing in a small group of healthy volunteers to determine if the drug is safe for people. (20-100 people)
  • Phase 2 Clinical Trial: Test in a small group of patients with a disease to evaluate drug effectiveness. (100-500 patients)
  • Phase 3 Clinical Trial: Test in a larger group of patients to determine safety, efficacy and risk/benefit (1,000-5,000 patients)
  • NDA: Submit New Drug Application to the FDA.
  • Manufacture the drug on a small or large scale
  • Phase 4 Trial: Pharma companies continue to monitor the drug and submit reports to the FDA re: any adverse effects.

Southern Research Names Alan Stokes Director of Toxicology and Pathology

BIRMINGHAM, Ala. –  April 6, 2015 – Alan Stokes, Ph.D., today joined Southern Research’s drug development division as the director of toxicology and pathology at its Birmingham headquarters. In this role, Stokes will manage groups of toxicologists, laboratory technicians, project team members, and formulation scientists for contracted studies in support of drug development activities.

“We are extremely pleased to have Dr. Stokes join the Southern Research drug development team,” said Andrew Penman, vice president of drug development at Southern Research. “He is bringing with him invaluable experience both in interacting with regulatory agencies and representing the non-clinical toxicology function for therapeutics at all stages of development.”

Stokes has more than 14 years of combined experience in pharmaceutical drug development for leading pharmaceutical companies including Schering-Plough, Wyeth Consumer Healthcare, and most recently, GlaxoSmithKline, where he was head of toxicology at Research Triangle Park, North Carolina.

He is a diplomate to the American Board of Toxicology, and he is a member of the Society of Toxicology, the American College of Toxicology, and the editorial board for the International Journal of Toxicology.

Stokes earned a doctorate in pharmacology with a focus on neurotoxicity from Wake Forest University and completed a post-doctoral fellowship at the Robert Wood Johnson Medical School Department of Neurology at Rutgers University.

About Southern Research
Founded in 1941 in Birmingham, Alabama, Southern Research is a not-for-profit 501(c)(3) scientific and engineering research organization that conducts preclinical drug discovery and development, advanced engineering research in materials, systems development, and energy and environment research. Approximately 500 team members support clients and partners in the pharmaceutical, biotechnology, defense, aerospace, environmental, and energy industries in facilities in Alabama, Maryland, North Carolina, Georgia, and Texas.

 

Southern Research Drug Development to Exhibit at SOT 54th Annual Meeting and ToxExpo

BIRMINGHAM, Ala. – March 11, 2015 – Southern Research – developer of seven FDA-approved cancer drugs – will be exhibiting at the Society of Toxicology (SOT) 54th Annual Meeting and ToxExpo, March 22 – 26, 2015, in San Diego, at booth #1301.

A science-driven, client-focused, preclinical contract research organization, Southern Research has more than 50 years of experience in drug development. Services include efficacy testing, with special expertise in anti-cancer drugs and anti-infective drugs (antibacterial and antiviral, supported by BSL-2 and BSL-3 laboratories and animal facilities), and a complete range of safety testing, including reproductive toxicology, with extensive bioanalytical, PCR and anatomic/clinical pathology facilities.

Utilizing comprehensive, in-house in vitro and in vivo capabilities, Southern Research’s experienced scientists work closely with clients in providing expert guidance and advice during all phases of preclinical development. A key hallmark of its program is the capability to provide custom-designed assays and studies to meet clients’ specific research needs.

In 2014, Southern Research, along with four other research organizations, formed the Southern Biologics Network (SBN) to create advanced biologics faster and less expensively for biopharmaceutical companies of all sizes. SBN provides comprehensive biologic development services, which include the manufacture, discovery, preclinical development, and early-stage clinical development of biologics.

Most recently, Southern Research expanded preclinical service offerings in drug development with the addition of GLP-compliant in vitro safety pharmacology testing on CytoPatch™. With the CytoPatch system, Southern Research successfully demonstrated in vitro hERG ion channel blocking by drug candidates at a physiologically relevant 37 degrees Celsius.

In addition to its scope of drug development services, Southern Research also offers pharmaceutical consulting in formulation, processing, manufacturing, and business operations.

Please visit Southern Research at booth #1301 to meet Director of Business Development Robin Akers, who will be able to answer your questions and discuss new business opportunities.

About SOT
Founded in 1961, the Society of Toxicology (SOT) is a professional and scholarly organization of more than 7,800 scientists from academic institutions, government, and industry representing the great variety of individuals who practice toxicology in the U.S. and abroad. SOT is committed to creating a safer and healthier world by advancing the science of toxicology. SOT promotes the acquisition and utilization of knowledge in toxicology, aids in the protection of public health, and has a strong commitment to education in toxicology and to the recruitment of students and new members into the profession. For more information about SOT and toxicology, visit www.toxicology.org.

About Southern Research
Founded in 1941 in Birmingham, Alabama, Southern Research is a not-for-profit 501(c)(3) scientific and engineering research organization that conducts preclinical drug discovery and development, advanced engineering research in materials, systems development, and energy and environment research. Approximately 500 team members support clients and partners in the pharmaceutical, biotechnology, defense, aerospace, environmental, and energy industries in facilities in Alabama, Maryland, North Carolina, Georgia, and Texas.

 

Southern Research Broadens Preclinical Services in Drug Development with CytoPatch™

BIRMINGHAM, Alabama – December 9, 2014 – Southern Research is broadening its preclinical service offerings in drug development with the addition of Good Laboratory Practices (GLP)-compliant in vitro safety pharmacology testing. Safety pharmacology testing relates to the study of potentially undesirable pharmacodynamic effects of a new product in both the in vitro and in vivo settings. Current methodologies include measuring ionic currents in cells over-expressing individual ion channels. In its GLP-compliant laboratories, Southern Research recently implemented an in vitro screening program on CytoPatch™ – the automated patch clamp platform – and successfully demonstrated in vitro hERG ion channel blocking by drug candidates.

This type of work has traditionally been conducted at room temperature, but with the CytoPatch™ system, Southern Research is able to operate at a physiologically relevant 37 degrees Celsius. Administering these studies at this temperature resulted in generally higher currents, leading to differences in the activity of the tested compounds. Work is ongoing to expand this service to other relevant ion channels, specifically, Kir 2.1, early and late Nav and Kv7.1mink. By using an automated system to perform these assays, the throughput of compounds and the reproducibility of data both increase.

Southern Research has a rich history of supporting preclinical drug discovery and development programs for a broad array of clients and has significant experience in generating study data that can be used to support regulatory submissions. The changing regulatory landscape, with respect to cardiac arrhythmia risk assessment, is of particular importance in drug development. There is a crucial need for systems that can effectively provide reliable data to make these assessments.

“We see a real need for service providers that can present clients with solutions to changing regulatory requirements and provide robust datasets to drive compound selection and development in the most cost effective and timely manner possible,” said Andrew D. Penman, Ph.D., vice president of drug development at Southern Research. “We firmly believe that there is a need for more relevant and robust systems that can be used to address the current preclinical testing paradigm, and Southern Research is currently focusing on investment in these areas.”

About Southern Research

Founded in 1941 in Birmingham, Alabama, Southern Research is a not-for-profit 501(c)(3) scientific and engineering research organization that conducts preclinical drug discovery and development, advanced engineering research in materials, systems development, and environment and energy research. Approximately 500 team members support clients and partners in the pharmaceutical, biotechnology, defense, aerospace, environmental, and energy industries in facilities in Alabama, Maryland, North Carolina, Georgia, and Texas.