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Tigecycline offers new hope in
the battle against MRSA
Study data presented at a major recent conference has demonstrated that Wyeth's
novel antibacterial tigecycline acts against drug-resistant pathogens in some
serious bacterial infections, including MRSA. While Wyeth will have to work hard
to establish tigecycline in this competitive area, its encouraging tolerability
profile could give it a useful advantage over existing treatments.
US pharmaceuticals company Wyeth presented a range of clinical data at the 44th
Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC) in
October, including Phase III data from a clinical trial in patients with
complicated intra-abdominal infections and from another in complicated skin and
soft tissue infections (cSSI). The first trial, which compared tigecycline to
Merck & Co's carbapenem Primaxin (imipenem/cilastin), found that a twice-daily
dose of tigecycline was non-inferior to a comparable regime of Primaxin. In
addition, adverse events occurred as often with Primaxin as with tigecycline,
with the most common being gastrointestinal in nature.
The tigecycline 305 cSSI trial compared 50mg of tigecycline, taken twice daily
after an initial loading dose of 100mg, to a twice daily regimen of 1g
vancomycin combined with 2g of aztreonam. Tigecycline was again found to be
non-inferior to the comparator regime demonstrating a lower incidence of serious
side effects, in particular raised alanine aminotransferase and aspartate
aminotransferase levels.
In addition to the Phase III trial data presented, Wyeth also provided details
of a number of in vitro resistance studies. The Tigecycline Evaluation
Surveillance Trial (TEST) examined the activity of the drug against a number of
resistant strains of bacteria, including methicillin susceptible staphylococcus
aureus (MSSA) and methicillin resistant staphylococcus aureus (MRSA). One study
found that tigecycline had good activity against clinical strains of
community-acquired MRSA and multi-drug resistant MRSA. Furthermore, oxacillin
resistant strains of staphylococcus aureus (ORSA) were also susceptible to
tigecycline.
New treatment option
The development of tigecycline, the first in the novel glycylcycline class, has
provided a new option in the ongoing fight against resistant pathogens,
particularly in severe or hospital treated infections. Although the drug's
efficacy against resistant strains of bacteria is a key advantage, Professor
Peter Hawkey, Professor of Public Health Bacteriology at the West Midlands
Public Health Laboratory, commented that its tolerability profile would also
help to position it favorably.
Currently, there are several injectable antibacterials available for the
treatment of resistant infections, such as Pfizer's Zyvox (linezolid), King
Pharmaceutical's Synercid (quinupristin/dalfopristin) and Cubist's recently
approved Cubicin (daptomycin). However, there are a variety of adverse effects
associated with these drugs, for example the development of myelosuppression
with the prolonged use of Zyvox. Professor Hawkey believes that this will ensure
tigecycline will not only establish itself in the treatment of severe
infections, but may also lead to it being used instead of some of the already
available narrow-spectrum drugs.
Recent Datamonitor research found that some of the newer, novel antibacterials
acting against drug-resistant pathogens tend to be reserved for use when other
options have been exhausted. There are several reasons for this, but primarily
it is due to the need to protect against the development of resistance to these
products. With so few drugs in the antibacterials pipeline, especially with
activity against gram-negative bacteria, physicians are wary of shortening the
useful life of newly launched drugs through premature resistance development.
The future use of tigecycline
A second reason is often the cost of the drugs, with many commanding a premium
price point due to the sizeable unmet need and their use in niche markets.
However, Professor Hawkey commented that, in reality, the cost-effectiveness of
these drugs is comparable to some other antibacterials, since associated costs,
such as longer hospitalization and additional nursing time, are reduced through
the drugs' rapid efficacy.
In a partial reflection of these concerns, recent Datamonitor key opinion leader
research in the seven major pharmaceutical markets found there were mixed
opinions regarding the future use of tigecycline in the hospital antibacterial
market: "It's about the only gram-negative that's actually offering anything new
just now, and even that is marginal," one opinion leader commented.
In an increasingly crowded market, Wyeth will have to strategically position
tigecycline to ensure maximum uptake in the hospital treatment market. Products
such as Zyvox, which offers the advantage of an IV/oral switch option enabling
earlier discharge from hospital, are already established in this segment and
real benefits will have to be demonstrated by tigecycline to encourage
physicians to switch. However, the data presented at the 44th ICAAC has gone
some way towards establishing the drug's utility in complicated bacterial
infections. Subsequent studies could be crucial in cementing that position.
Related research:
•
Commercial Insight: Antibacterials - Regulations, Resistance & Generics
•
Stakeholder Insight: The Hospital Antibacterial Market - Specialist Products
Drive Market Growth
•
Pipeline Insight: Antibacterials - Select Classes, Select Uses
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