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Printable Handouts
Navigable Slide Index
- Introduction
- Tuberculosis history
- Pre-1946
- The streptomycin trial
- The streptomycin trial – the long term results
- Headlines in tuberculosis drug development (1)
- Headlines in tuberculosis drug development (2)
- Standard treatment for drug-sensitive TB
- Toxicity
- Treatment duration
- Challenges in TB treatment
- Some examples of drugs in development
- New trials to shorten treatment for TB
- Fluoroquinolones for TB
- Johns Hopkins study
- REMoxTB study objective
- Hypothesis
- Primary study endpoints
- Study design
- Visits
- Overview of TB microbiology protocols
- Safety
- REMoxTB status
- REMoxTB current status
- Gatifloxacin project: phase III (1)
- Gatifloxacin project phase III: treatment & follow-up
- Gatifloxacin project: status
- Trial design rifaquin
- Rifaquin outcome reported at CROI
- Summary of fluoroquinolone studies
- More TB drug development approaches
- New combination regimen studies
- NC-001 conclusions
- NC-002 current status
- MAM- multi arm multi stage
- Advantages of MAMS-TB
- Risks of MAMS-TB
- MAMS-TB design
- MAMS-TB current status
- Developing new treatments for MDR/XDRTB
- Current WHO treatment for MDRTB
- Creating an MDR TB regimen
- Using existing and repurposed drugs
- Linezolid in refractory XDR tuberculosis
- New drugs for MDRTB (Delanamid)
- New drugs for MDRTB (Bedaquinline)
- Drugs in development for MDR indication
- Summary
- Acknowledgements
Topics Covered
- Tuberculosis history
- The streptomycin trial
- Headlines in tuberculosis drug development
- Standard treatment for drug-sensitive TB – Toxicity
- Treatment duration
- Challenges in TB treatment
- Some examples of drugs in development
- New trials to shorten treatment for TB
- Fluoroquinolones for TB
- Johns Hopkins study
- REMoxTB study objective
- Overview of TB microbiology protocols – Safety
- Gatifloxacin project: phase III
- More TB drug development approaches
- New combination regimen studies
- MAM- multi arm multi stage
- Developing new treatments for MDR/XDRTB
- Current WHO treatment for MDRTB
- Using existing and repurposed drugs
- New drugs for MDRTB (Delanamid, Bedaquinline)
- Drugs in development for MDR indication
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Gillespie, S. (2014, April 2). Tuberculosis: new treatments in evolution [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/VGRO1114.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Stephen Gillespie is in receipt of research grants from MMRC, EDCTP, Global Alliance for TB Drug Development. Professor Gillespie’s involvements in clinical trials are supported by active and placebo drug supplies from Bayer Schering Health Care and Sanofi Aventis, while also providing support with regulatory and drug safety advice. Neither company has a managerial role within the study, however. Professor Gillespie has also provided training to senior staff at Bayer Schering Health Care.
A selection of talks on Microbiology
Transcript
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0:00
Tuberculosis-- New Treatments in
Evolution by Stephen Gillespie,
Professor of Medicine at the
University of St. Andrews.
In this presentation, I will
outline a little of the history
of anti-tuberculosis chemotherapy
and tell you something
of the exciting new studies
that are currently underway.
0:21
Tuberculosis is an ancient disease.
It was described by
Hippocrates, who recognized
that this disease was untreatable.
Avicenna recognized that
tuberculosis was contagious.
And he advised that patients
should be put into quarantine.
This concept was developed
further by Herman Brehmer
in the 19th century,
who developed what
is known as the Sanatorium Movement.
This approach was widely
adopted across Europe
with most cities opening
sanatoria for TB treatment.
Most of them were not
closed until the 1970s.
In the 1880s, there were campaigns
in the United States and the United
Kingdom to raise
awareness of tuberculosis.
Public health notification
was established.
And public information campaigns
advising against coughing
and spitting were placed
in public transport.
1:14
In the early antibiotic era,
research showed that tuberculosis
was not susceptible to
the newly available drugs.
Many thought that this was due
to the complexity of the organism
and that tuberculosis might
prove too difficult to treat.
At this time, there were many
other potential cures including
pelargonium roots, a Zulu treatment
for respiratory infection.
Cod liver oil was thought to be
useful in preventing the disease.
Gold was applied by some physicians
with a degree of success.
But many patients
experienced toxicity.
It was the discovery by Selman
Waksman and Albert Schatz
of streptomycin that revolutionized
tuberculosis chemotherapy.
In the United States,
this drug was introduced
into practice without
clinical trials.