Article

Hospital Injectable Drugs: Future Prospects for Generics & Biosimilars

Topic: Biofeedback and NeurofeedbackPublished July 29, 2011

Legacy signals

Legacy popularity: 3,135 legacy views

The generic injectables sector exceeds US$11.2 billion and numerous high-value injectable products will face patent expiry in major markets over the next decade. This critical new report evaluates the markets, players and products in detail. Browse All: Pharmaceutical Market Research Report As companies seek new ways to gain a competitive edge in maturing generics markets, injectables have become increasingly desirable to the major players. Companies like Teva, Sandoz, Mylan, Hospira and Hikma have all increased their presence in the injectables sector through acquisitions in the last couple of years. And interest has not been limited to established generic companies, as pharmaceutical majors like Pfizer have also become attracted to the generic injectables market. High risks, high reward This is hardly surprising with a global injectables market in the region of US$120 billion. While the lion’s share remains with the innovative industry for the time being, the generic injectables sector already exceeds US$11.2 billion and numerous high-value injectable products will face patent expiry in major markets over the next decade. But, many of the big sellers are biological products and biosimilar approvals will only be possible for a few companies. Gaining regulatory approval in developed markets is more complex for biosimilars. For companies who are able to navigate the approval process, the sector for biosimilars is inherently different to the traditional generics market. Market acceptance remains a big challenge and the take-up of biosimilars in Europe has been relatively slow. Not only will companies need to convince healthcare providers that biosimilar drugs are as good as the originator products, they will also have to compete with the originator companies who are unlikely to exit the market as they may previously have done when faced with a flood of bioequivalent generics. Is a biosimilar market inevitable?rnThe fact remains that the generic drugs sector must either respond vigorously or rely on a diminishing number of non-biological products. Progress to developing a biosimilar market to date has been patchy and slow, and few competitive therapies are beyond early-stage research. But accessing the fast-growing hospital market will be essential. Health payers, the branded industry and investment community will all be watching developments closely. A complete analysis packed with market facts,product forecasts to 2016 and detailed company evaluationsrnAbout the author: The report has been researched and written by Espicom’s Senior Pharmaceuticals Analyst, Karen Holmes. Karen has over 15 years pharmaceutical and healthcare market analysis experience. Her recent studies include Injectable Generic Drugs: Prospects and Opportunities, Emerging Opportunities in Inhalation and Nasal Spray Generic Drugs, and Ophthalmology Drug Futures. Related Reports: Global Injectable Drug Delivery Market (2010 - 2015) Generic Drugs in consumer health global overview 2011 Contact:rnMr.Priyankrn7557 Rambler road,rnSuite727,Dallas,TX75231rnTel: +1-888-989-8004rnE-mail: sales@reportsnreports.comrnhttp://www.reportsnreports.com

Further reading

Further Reading

4 total

Article

The main focus of drug carrier research today is to identify carriers that are both safe and effective for clinical treatment applications. As treatment strategies advance researchers regularly update drug delivery systems. Traditional drug delivery systems consist of liposomes and polymer micelles together with nanoparticles but despite their inclusion in clinical trials current versions still encounter limitations. Liposomes struggle to release hydrophobic drugs from their

March 26, 2025

Article

Traditional immunoassays based on the format of 96-well microtiter plates are widely used in analytical laboratories and have become increasingly automated with the introduction of robotics technology in recent years, thereby enhancing assay throughput. Most clinical analyzers essentially operate as "stand-alone laboratories," featuring precise, accurate, and highly reproducible programmatic liquid handling, sample addition, and washing steps. However, aside from cost, the si

March 26, 2025

Article

The History of ADC Drugs ADC drug history begins with "magic bullet". Physicians have long had high cytotoxic chemotherapy drugs for tumour treatment. As they target cancer cells, chemotherapeutics will also random attack healthy cells and become systemically toxic. Paul Ehrlich came up with the term "magic bullet" in 1913. He pictured fitting chemotherapy drugs on carriers that would shoot to tumour cells – as they do with missiles – to send them to tumor tissue so that

March 26, 2025

Article

The primary function of atrial natriuretic peptide ( ANP/a>) includes regulation of water and salt metabolism together with vascular volume which helps control blood pressure stability. Additionally, ANP manages endothelial cell permeability and counters the adrenal aldosterone system which allows it to control growth metabolism and influence myocardial hypertrophy and fibrosis regulation. Recent research shows that ANP and its receptors are present in several immune cells an

March 26, 2025