Showing posts sorted by relevance for query parexel. Sort by date Show all posts
Showing posts sorted by relevance for query parexel. Sort by date Show all posts

Friday, June 13, 2008

PAREXEL buy ClinPhone

PAREXEL announced that the Boards of PAREXEL International and ClinPhone plc, a company traded on the London Stock Exchange, ("ClinPhone") have reached agreement on the terms of a recommended proposal whereby awholly owned subsidiary of PAREXEL will acquire the entire issued and to beissued ordinary share capital of ClinPhone.

With headquarters in Nottingham, United Kingdom, ClinPhone is one of the world's leading clinical technology organizations. The acquisition is based on the offer price of 135 pence in cash for each ClinPhone share. The offer price represents a premium of 86 percent to the ClinPhone share price on the London Stock Exchange of 72.5 pence.

More

UPDATE: Quintiles Transnational, a U.S.-based pharmaceutical services company, is weighing a counterbid for Britain's Clinphone (CNP1.L: Quote, Profile, Research, Stock Buzz) that would trump an $182 million agreed bid from biotech firm Parexel International (PRXL.O: Quote, Profile, Research, Stock Buzz).

Sunday, April 27, 2008

Parexel get an apology from The Sunday Express

"The World's Greatest Newspaper" now writes:

On 13th April we published an article which incorrectly claimed that two volunteers were hospitalised after participation in an ongoing clinical trial run by PAREXEL International.

In fact, we now accept that the incidents mentioned related to a significantly different version of the study drug and trials conducted in the USA in 2000 and 2002 by a company unconnected to PAREXEL.

Monday, December 15, 2008

PAREXEL - file in the "irony drawer"


PAREXEL, the company who ran the TGN1412 "elephant man" clinical trial, has been named the "Best Contract Research Organization (CRO)" by Scrip World Pharmaceutical News. The award was presented to PAREXEL at the fourth annual Scrip Awards ceremony held on December 10, 2008 in London, England. The Scrip Awards are designed to celebrate innovation and a continued commitment to improving healthcare worldwide.

Thursday, March 16, 2006

Parexel - TGN 1412; First and last time into man?

Six men have been admitted to the intensive care unit of a North London hospital after suffering a severe reaction to an antibody administered in a Phase I clinical trial.

The men had volunteered for a study of a compound called TGN1412, in development by German biotechnology company TeGenero as a treatment for chronic inflammatory diseases and leukaemia.

Shortly after being dosed with the drug, the men experienced multi-organ failure and two are said to be critically ill. Two other men who received placebo were unharmed.

The trial was being conducted by contract clinical research organisation (CRO) Parexel, which owns and operates the dedicated clinical research facility unit at the Northwick Park Hospital where the trial took place.

The statement from Parexel about this tragedy can be read here.

Roy Poses at Health Care Renewal has written a number of times recently about US contract research houses.

His concerns have been to do with quality standards.

Insider is in no way implying that this was an issue in this case. But it will be interesting to see what the, now inevitable, enquiry turns up.

Some questions Insider would raise would include: the rationale for dose selection; the Ethics Committes' review of the protocol; experiences with similar compounds and finally the animal toxicity data.

Tuesday, April 15, 2008

Parexel correct The Sunday Express

Boston, MA, April 14, 2008 – Over the weekend the Sunday Express newspaper in the United Kingdom published an article that contained false and erroneous information. The article incorrectly claimed that two volunteers were hospitalized after participating in a clinical trial, involving a pharmaceutical product being developed for the treatment of addictions, at a PAREXEL U.K. site.

This report is completely inaccurate. In fact, the study is running smoothly without incident.

Source

Monday, September 25, 2006

Parexel - TGN 1412: TV show revelations leaked to press

The victims of the catastrophic TGN 1412 'Elephant Man' clinical trial were given the test drug at a 'reckless' rate, according to experts.

The drug, designed to fight leukaemia, rheumatoid arthritis and multiple sclerosis, was injected 15 times more quickly than when given to monkeys in animal studies, confidential documents have revealed.

Leading scientists believe this 'reckless' mistake could explain the horrendous reaction to the drug which left volunteers fighting for their lives.

The six young men - all fit and healthy before signing up for the March trial at Northwick Park Hospital in North-West London - suffered a host of side-effects, including pain, vomiting and organ failure.

Bar manager Mohamed 'Nino' Abdelhady, 28, was described as 'the Elephant Man' by his partner Myfanwy Marshall after his head swelled up.

Trainee plumber Ryan Wilson, 20, suffered heart, kidney and liver failure, pneumonia and blood poisoning and was in a coma for three weeks.

While in the coma, he suffered a frostbite-like reaction and has since lost parts of his fingers and had his toes amputated.

The volunteers, who are launching a multimillion pound damages claim against Parexel, the private research firm that ran the trial, face the risk of contracting cancer and other chronic and incurable diseases such as multiple sclerosis.

TeGenero, the company who were developing TGN1412, have already gone into liquidation.


The UK TV programme "Dispatches: The Drug Trial That Went Wrong" will be on Channel 4 this Thursday at 9pm.

Daily Mail

The Sunday Times has more detail.

Sunday, April 13, 2008

Parexel - clinical trials, ain't they a bitch!?




TWO volunteers are in hospital after taking experimental drugs being tested by the company which ran the disastrous "Elephant Man" drug trials two years ago.

The controversial US giant Parexel has been recruiting “guinea-pigs” to test a potentially dangerous new drug designed to help people overcome addictions.

Two have been taken to hospital suffering from potentially deadly conditions after taking nalmefene.

More at The Sunday Express

Wednesday, July 05, 2006

TGN 1412 - Te Genero throw in the towel


The German biotech company whose drug TGN 1412 put two UK men in a deep coma following their participation in a clinical trial has announced it is going into liquidation.

TeGenero, who produced the drug, which was disastrously tested by US firm Parexel earlier this year, said its insolvency had come as a direct result of the negative publicity generated by its case.

The firm's failure to attract investors for future funding was caused by the substantial press coverage the case attracted, TeGenero explained in a statement.

More here.

Insider's view: and how does this leave the poor trial volunteers and their hopes of any (completely justifiable) compensation. At least one of the volunteers is facing surgery on damaged fingers and toes (picture).

One hopes Parexel will now step upto the plate and do the right thing.

Let's see!

Thursday, June 17, 2010

Big Pharma's stalled R&D machine - By BEN HIRSCHLER and KATE KELLAND, Reuters

LONDON - At just 28, Duncan Casey has already been from the university science bench to the world of Big Pharma research and back again. Now working in an Imperial College lab tucked behind London’s famous Science Museum, he has no illusions about the prospects for researchers in the pharmaceutical industry.

“The unit I used to work in — GlaxoSmithKline’s place in Harlow — has been closed down now,” says Casey, dressed in signature protective goggles and white coat as he works on synthetic chemistry. “It used to be a job for life. Now it’s a job until the next restructuring.”

Across the western world, Big Pharma is cutting back on the number of scientists it employs in its labs and the money it spends on research and development. The hunt for new drugs continues, but the men and women in white coats — traditionally viewed as the lifeblood of the industry — are not as untouchable as they once were.

It’s a similar story at GlaxoSmithKline’s research laboratories in Verona, where lunchtime conversations can be decidedly gloomy. Glaxo is axing the Italian facility, shedding 500 jobs as part of a programme of cuts designed to improve returns on R&D. Many scientists feel stranded or wonder why they entered the profession at all.

“It’s a sad but true fact that science really doesn’t pay any more,” says one young researcher who would not give her name for fear of jeopardising her future prospects in the industry. “The lunchtime discussion today was about what we’d go back and study if we were 18 again and choosing university courses. There were only a few of us who said they’d still go for a science degree.”

Across the Atlantic in Cambridge, Mass., Adrian Ivinson, director of Harvard’s NeuroDiscovery Center, is reminded of the shifts underway in the industry every time he looks out of his window. Over the road, the “gorgeous, state of the art labs””no longer house Merck & Co Inc’s neuroscience team. “They only built it a few years ago and had this wonderful neuro group in there,” Ivinson says. “Now they’re gone.”

The magnitude of the changes is hard to ignore.

U.S. drug giants Pfizer Inc and Merck have slashed thousands of jobs since acquiring smaller rival firms last year. British-Swedish firm AstraZeneca has plans to close its research labs at Charnwood in central England by the end of 2011, with the loss of up to 1,200 jobs; its Swedish research unit in Lund will also shut. In Japan, Astellas Pharma Inc has announced plans to limit its research expenditure.

Sam Isaly, managing partner at OrbiMed Advisors — with some $5 billion under management it is one of the world’s largest healthcare investment firms — expects employment in the 14 Big Pharma companies across the United States, Europe and Japan to fall around 20 percent between 2009 and 2015. That means some 200,000 jobs will disappear across the drugs business — not only in research but also in sales and back office functions. “The management of these companies have to deliver to their shareholders, so they are downsizing or making acquisitions or diversifying,” says Isaly.

NEW PRODUCTS, NEW MARKETS

One factor forcing Big Pharma to rethink its business model is the huge number of patents that are set to expire over the next five years. As patents run out on blockbuster prescription tablets like Pfizer’s $12 billion-a-year cholesterol medicine Lipitor and AstraZeneca’s $5 billion heartburn pill Nexium, cut-price generics are sure to rush in and slash margins. Between now and 2015 products with sales of more than $142 billion will face copycat competition, according to IMS Health, the leading global supplier of prescription drug data. It is the biggest “cliff””of patent expiries in the history of the pharmaceuticals industry.

Add in tougher regulatory hurdles and a brutal squeeze on healthcare budgets as cash-strapped governments push austerity programmes and it’s little wonder that drug companies are cutting back and shifting focus.

The strategy so far has been to buy promising new drugs from outside developers and boost investment in the relative safety of non-prescription consumer products. Big drugmakers are also moving into new markets — with Asia at the top of everybody’s list. It all adds up to a redesign of the multinational pharmaceutical company. In the 21st century, says Isaly, Big Pharma will primarily be a distribution business.

HORLICKS HELPS CEO SLEEP AT NIGHT

A peek inside the bag of free goodies handed out to shareholders at Glaxo’s annual meeting in London gives an idea of one direction the industry is headed. Aquafresh toothpaste, Corsodyl mouthwash, Breathe Right nasal strips and Lucozade energy drink are not exactly at the cutting edge of bioscience, yet they are all products that now enjoy top billing under Glaxo’s youthful Chief Executive Andrew Witty.

Under Witty, who has been in the top job for two years, over-the-counter remedies, oral care and health drinks have become a key pillar of Glaxo’s drive to reduce reliance on traditional prescription pharmaceuticals. As if to emphasise that fact, the one new hire highlighted by the CEO in his address to the meeting was Emma Walmsley — an executive poached from French cosmetics group L’Oreal SA and heir apparent to run Glaxo’s reinvigorated consumer healthcare business.

Glaxo may be working on groundbreaking treatments for cancer, but one of Witty’s favourite products is Horlicks, a malted milk powder best known in Britain as a bedtime drink for the elderly. Horlicks is a huge seller in the key emerging market of India. The brand clocked up 146 million pounds ($214 million) in Indian sales in 2009, bagging an enormous 48 percent of the hot drinks market there.

For industry veterans like Andy Smith, who worked at what was then SmithKline Beecham in the 1990s and is now a healthcare fund manager at Axa Framlington, the change is profound. “When I worked for consumer healthcare we were always the poor relation, which is actually why I moved to the pharmaceuticals division,” he says. “Senior management always used to complain about the mixed P/E (price-to-earnings) multiple of having a consumer healthcare business and a pharmaceutical business and the fact that the analysts didn’t understand it — but now they are really appreciating it.”

It’s not hard to see why. Ten years ago, the pharmaceutical sector was trading at 30 times expected earnings. Today, most Big Pharma shares have a forward P/E of under 10, while consumer products companies like Procter & Gamble Co fetch around 15 times forecast earnings.

But diversity doesn’t just mean selling a wider range of products. Big western drugmakers are also expanding into emerging markets such as China, which is set to overtake Germany as the world’s third biggest drugs market next year, according to IMS. The fast-expanding middle classes in China and elsewhere are demanding drugs that they couldn’t afford a few years ago. Overall sales growth in emerging markets is expected to be three times that of developed markets in the next five years.

In China, western companies have linked up with local players and research institutes. Some firms are even cosying up to old enemies in the Indian generics sector, following new legislation that has improved patent protection in that country.

But multinational drugmakers know they have to do more than sell toothpaste and expand into Asia. They need more and better drugs to sell — and they need them fast.

REVERSE ALCHEMY

The problem is, Big Pharma doesn’t have nearly enough new drugs in the pipeline to replace all those it is about to lose. Since 1950 — virtually the dawn of the modern era of medicine — a total of 1,256 new drugs have been approved by the U.S. Food and Drug Administration (FDA). But the industry today produces roughly the same number of new medicines that it did 60 years ago.

Ten years ago there was a lot of hope that process-led research systems would industrialise the hunt for new drugs. But that optimism may have been misplaced. A spike in drug approvals in the mid-1990s, it turns out, was not the result of any fundamental improvement in productivity but largely down to the FDA clearing a backlog of applications after the introduction of a new system under which companies paid “user fees””to help speed the process.

Despite pouring billions into research — more than $65 billion last year in the U.S. alone — the number of new drugs launched annually has fallen 44 percent since 1997, according to CMR International, a Thomson Reuters subsidiary.

Big Pharma has also struggled over the past decade to produce the kind of big new hits that make the bulk of its money. As with other industries dominated by blockbusters — think Hollywood movies or oil and gas exploration — it’s not easy to pick winners years in advance. Even after a drug gets approval, commercial success can be a hit-and-miss affair, as evidenced by lacklustre sales of recent arrivals such as the keenly anticipated blood-thinner Effient from Eli Lilly and Co and Daiichi Sankyo Inc.

“Once you take into account all the drugs that have fallen by the wayside, the returns have been pretty bad,” says Peter Fellner, a veteran with three decades experience in both pharmaceuticals and biotechnology. “It is a reverse alchemy calculation where you are taking a very large amount of gold and quite rapidly transmuting it into lead.”

Few people understand the current change better than Fellner. After working for Swiss drugs giant Roche Holding AG in the 1980s, he headed up Britain’s flagship biotech company Celltech. Now the quietly spoken management veteran chairs a clutch of small drug development and medical technology companies.

The move to cut R&D, he says, is one of the most profound changes in the industry in decades. Some firms are pulling back from problematic areas like depression, where proving the value of new medicines in clinical trials is fiendishly difficult. Lack of progress in this field is a prime reason behind Glaxo’s decision to cut research in Verona. Other firms are cutting back in areas that used to be their bread and butter. Pfizer, for instance, is trimming research into cardiovascular drugs and AstraZeneca is ending discovery in psychiatric medicine.

Instead of pouring money into R&D themselves, drugmakers are turning to smaller firms, outsourcing routine research functions and even buying in smart blue-sky discovery work.

Some scientists fear that shift will strip drug companies of the creative talent that has driven the industry for decades. But it is good news for contract research organisations (CROs) like U.S.-based firms Covance Inc and Charles River Laboratories International Inc, which saw their shares soar — at least until late 2008, when the recession and the scale of the structural problems facing the pharmaceuticals industry forced many smaller drugmakers to abandon certain areas of research altogether. Despite the setback, big CROs expect to expand in the long-term and are investing heavily in drug discovery services.

BRAIN SHIFT

They’re also happy to pick up Big Pharma’s leftovers. Glaxo, for example, is negotiating to sell its Verona site to a U.S.-based CRO called Aptuit. Parexel International Corp, which is based in Boston and conducts clinical trials for drugmakers around the world, is busy hiring hundreds of new staff — many of them refugees from Big Pharma. “It’s a brain shift,” says Parexel’s chief executive and founder Josef von Rickenbach. “The rate of outsourcing has continued to tick up pretty much every year across all clinical trial activities.”

How far can it go? Does it make sense for big drugmakers to simply throw in the towel on early-stage research and instead buy in promising products from smaller operators in the biotech sector? “In the current phase of the cycle, I think you will see companies come close to it,” says Fellner.

The short-term commercial case is compelling. Morgan Stanley analysts calculate that $1 invested by a big drugmaker in a product licensed from outside researchers will, on average, deliver three times as much value as the same dollar invested in in-house research. Some of today’s top drugs started life in outside labs, including AstraZeneca’s cholesterol fighter Crestor and Bristol-Myers Squibb Co’s schizophrenia drug Abilify.

While the immediate reasons for exiting some areas of R&D may be clear, though, the long-term implications are harder to know. There are obvious practical considerations. For one thing, pharmaceutical companies will need to make sure they retain enough internal know-how that they can continue to properly assess new drug prospects pitched to them by outside firms.

There are also significant reputational issues. Drug companies have long promoted the idea that they pursue new drugs for the good of humanity; it’s an argument Big Pharma regularly uses to justify the huge profits it makes. High returns, the industry argues, can be ploughed back into research on the next medical breakthrough. If Big Pharma is not doing the research itself, will the big margins be harder to defend?

Glaxo’s Witty says it’s all about balance. “We’d like to have a decent western, white pill business but I don’t want any part of the group to be overwhelmingly important. I want a balanced organisation,” he told Reuters. “I’d feel very comfortable if in a few years’ time ... we had a quarter of the business in that traditional pharmaceutical space, a big chunk of business in vaccines, a big chunk in consumer products and a big chunk in emerging markets, with new large molecules (biotech drugs) also coming through.”

A BIOTECH FUTURE — PERHAPS

There’s also a question of control. One hunting ground in the new-look world of Big Pharma is biotechnology. Biotech start-ups contribute an increasing share of the experimental compounds entering the development pipeline. Biotech’s “large molecule””protein drugs, made using genetic engineering, have proven superior at fighting complex diseases like cancer to many conventional “small molecule””chemical drugs.

By 2014, the world’s two top-selling prescription drugs won’t be tablets sold in blister packs but needle-based biotech treatments — Avastin for cancer, sold by Roche, and Humira for rheumatoid arthritis, from Abbott Laboratories — according to consensus forecasts compiled by Thomson Reuters.

But while biotech is attracting increased interest from large pharmaceutical firms, the sector is struggling with its own problems. Early funding is hard to come by and there’s growing scepticism from investors because of the huge risks involved in researching something that might never pay off. “Theoretically, this should all be good news for biotech because it means that Big Pharma is looking round more intensively for good pipeline opportunities,” says Sijmen de Vries, chief executive of Dutch biotech firm Pharming Group NV. “The reality is different. Financially, much of biotech is in a bad state of health because of the extremely unhealthy situation that exists at the moment with regards to investing in things that have even remotely the word ‘risk’ associated with them.”

De Vries, a straight-talking Dutchman who trained as a doctor before working at Novartis AG and SmithKline Beecham, knows all about risk. His company lies at one of the extreme edges of biotechnology and is pinning its hopes on a drug derived from the milk of genetically modified rabbits. The company hopes the milk can help a small group of patients with a rare genetic disorder, hereditary angioedema, which causes acute and painful swelling of the body’s soft tissues. European regulators could announce their verdict on the drug this month. If the drug is approved, the company should thrive. If it’s rejected, Pharming will struggle. Such binary events are typical in biotech.

All that puts biotech firms into something of a financial Catch-22. As Big Pharma cuts its R&D, it is looking to small independent companies such as biotech start-ups to fill the gap. But without financial backers to help develop new drugs through those early stages, those smaller firms struggle to survive. “Pharma companies are very good at certain things but the thinking-outside-the-box, early-stage stuff is generally better done in biotech than in pharmaceutical companies because pharmaceutical companies tend to be more conservative,” says Steve Jackson, professor of biology at the University of Cambridge. “The problem with that model is that venture capital funding is becoming more difficult to come by for biotech companies ... so that is another threat to the pharmaceutical companies’ pipelines. I’m not sure how many new biotech companies are going to be springing up over the next five years or so.”

Jackson has first-hand experience at how tough it is to shepherd a drug through those first few years. In the 1990s, he developed a cancer drug that prevents certain DNA repair proteins from working. That led to the creation of biotech company KuDOS in 1997. Finance was tough, but persistence and a winning idea eventually secured him three rounds of venture capital funding and, in 2005, the company’s sale to AstraZeneca. Today, he is looking to start another biotech business but finding times much harder. Ironically, while his original cancer drug is continuing to show promise in clinical trials, the KuDOS facility in Cambridge is now one of those facing closure as a result of the AstraZeneca cuts.

ONE LAST REFUGE

Back at Imperial College, Nick Brooks, a scientist working on membrane biophysics, scrutinises a computer screen showing the results of X-ray diffraction. For now, academia remains a refuge from change.

“Certainly, at the moment, the prospect of getting your job taken away is a lot less severe here than it is in the pharmaceutical industry,” he says.

He wonders how far the drug industry can change before it loses its science core — and its way. “I can’t help but feel that the idea of a pharmaceutical company having good researchers in-house to be able to take part in the whole process from conception of a drug through to marketing must be a benefit,” he says, before turning back to his work.

(Additional reporting by Julie Steenhuysen in Chicago and Bill Berkrot in New York; Editing by Simon Robinson and Sara Ledwith)
http://cnews.canoe.ca/CNEWS/World/2010/06/16/14417751.html?cid=rssnewslast24hours

Wednesday, April 07, 2010

AstraZeneca - Seroquel: the MDL players

This Multi-District Litigation consolidates a number of pending actions against UK-based AstraZeneca Pharmaceuticals, the maker of Seroquel, an antipsychotic medication used to treat schizophrenia and bipolar disorder. The plaintiffs allege that AstraZeneca failed to test and to warn users of the drug's alleged harmful side effects, including the risk of diabetes and related medical complications.

The company has been sued in U.S. courts by thousands of individuals who allege that the growth in sales of Seroquel, from $66 million in 1998 to $2.75 billion in 2005, was spurred by "AstraZeneca's aggressive marketing of Seroquel," which "consisted chiefly of overstating the drug's uses and benefits (including massive off-label promotion), while understating and consciously concealing its life-threatening side effects."

The following are the names and job titles of the people giving the depositions from which the documents come:

  • Tony Zook - President and CEO of AstraZeneca US (2006 to present); Senior VP, Commercial Operations (2001-2006); VP Marketing & Sales (1997-2001)

  • Jack Schwartz - Executive Director, Seroquel Development

  • Athena Ruhl - Seroquel Senior Product Manager

  • Michael Reinstein - Key Opinion Leader

  • Claudia Piano - Parexel

  • Charles Peipher - Marketing

  • Alfred Paulson - Sales

  • Henry Nasrallah - Key Opinion Leader

  • Jamie Mullen - Senior Director, Clinical Research

  • Kevin McKenna - VP, Regulatory Affairs, Neuroscience Therapeutic Area

  • Wayne Macfadden - Former Director Clinical Research and U.S. Physician for Seroquel

  • Gerald Limp - U.S. Regulatory Affairs (Deceased)

  • Marianne Jackson - National Sales Director

  • Jeffrey Goldstein - Former Director of Clinical Science

  • Wayne Geller - Former Global Drug Safety Physician (GDSP) for Seroquel

  • Susanne Fors - Global Regulatory Affairs Director

  • Vikram Dev - VP of U.S. Drug Safety

  • David Brennan - Chief Executive Officer, Chairman of the Senior Executive Team (SET)

  • Martin Brecher - Former Medical Science Director

  • Geoffrey Birkett - Former Vice-President Global Marketing

  • Donald Beamish - Commercial Brand Executive Director

  • Barry Arnold - EU Qualified Person for Pharmacovigilance (January 2006 to present); VP Clinical Drug Safety (July 1999 - May 2006)

See all documents related to the Seroquel Products Liability Litigation.

See related resources and articles.

Thursday, February 26, 2009

AstraZeneca - Seroquel: oh wow!

What a great read!

"From 2001 to 2006, Dr Wayne Macfadden was the US medical director for Seroquel and director of clinical research for central nervous system efforts by AstraZeneca. In a deposition in the case in 2008, given under oath, Macfadden admitted to a lengthy sexual relationship with a researcher at the Institute of Psychiatry, King's College in London, England and with a ghostwriter who worked at Parexel MMS (Medical Marketing Services) in the US, according to court records. Neither woman is named in court papers, due to the obviously sensitive nature of their dealings with Macfadden. Both women were intimately tied to publications favorable to Seroquel and AstraZeneca, according to court records."

Thursday, March 19, 2009

Pharma Giles writes .......


Pussy for Pills – the true story so unbelievable they said it could never be made into a movie. Coming to a cinema near you.

The story so far…


Florida. September. Wayne looked out of the window of his luxury hotel penthouse suite and let his gaze wander across the distant sun-drenched beach to the sunlit horizon.

He smiled.

Life was good, and a $200,000 salary plus expense account to match went a long way towards keeping it that way. Sure, being a top gun medical director for AstraZeneca was demanding. Very demanding. But there were plenty of rewards.

Wayne turned that thought over in his mind and laughed quietly to himself. He turned his eyes from the rolling, golden curves of the sand dunes and back to the rolling, golden curves of Redacted, who was pacing back and forth in the room behind him.

Make that physically demanding, he thought.

“Just tell me what you want, Wayne,” she said, worrying a blood-red finger nail. “Tell me what you really want.”

Time to get back to work, Wayne realised. He shivered.

“Honey, what I’d really like is for you to turn the air-con down,” Wayne replied. “It’s freezing in here.”

Redacted’s flimsy, figure-hugging dress revealed a couple of tell-tale signs, signs of either the artificially cool apartment breeze or her aura of barely-suppressed excitement. Wayne suspected they were due to the latter.

“Wayne, you just don’t understand,” she sighed. “Industrial espionage isn’t my scene. I’m just a silly little clinical researcher at silly little Parexel. What possible use am I to a high-flyer at AZ like you?”

Wayne stood up sharply and took three short, quick strides across to where Redacted was standing. He seized her long, copper-coloured hair and pulled her tight to him.

“Stop it! You’re hurting me,” she squealed. Then… “Don’t stop….”

He kissed her savagely, crushing her mouth to his lips, and felt her tremble with hot, needy desire.

“You’ve got something I want,” he purred. “Times, dates, results. You know. And in return, I’ve got something you want…”

He felt her hand reach feverishly for his belt.

“No, not that,” he laughed. “Not yet, anyway…”

She smiled. “Did you bring them?”

“They’re in the drawer, by the bed. The small blue bottle.”

Redacted smiled and turned away into the bedroom. Wayne heard her open the drawer and take out the vial holding the three precious Vicodin tablets. Her reward for being such a good girl, he reflected.

Yes, such a good girl. Just like all of the others.

Wayne thought back to the early days. AZ had always been one long party. He remembered the corporate excesses of his old US CEO, good ol’ Lars. Now there was a guy who really knew who to party.

He smiled at the memory. Even back then, Wayne had acquired a reputation as a Don Juan amongst medical researchers. Love ‘em, lay ‘em, leave ‘em. Back then of course, such behaviour was perfectly acceptable, even encouraged and certainly greatly admired, even by the ladies.

His abilities in that sphere of research operations had not gone unnoticed by senior management, either.

“Zere iz nozzing wrong viz using your greasy pole to help climb ze greasy pole,” Lars himself had once joked to him.

Great days, great days. All different now, of course. Political correctness had forced out Lars long ago. And most of the characters like him.

“Not the anything has really changed,” Wayne’s former marketing colleague Mike Zubillaga had once said to him. “You can still pull the same old stunts to get results. The only thing is that now, if you get caught, your management will cut you off at the knees. They feel they have to pretend that they don’t know what really goes on. If it’s all going well, then fine, but if Joe Public finds out what you’re up to, then it’s goodbye. No way will an executive take a bullet in support of guys like us, these days.”

And boy, did Zube ever find that out the hard way, reflected Wayne…

“What are you thinking about, Wayne?” cooed Redacted, interrupting his reverie.

She was standing in the bedroom doorway, wearing a translucent white cotton hotel bathrobe. Her long, tanned legs carried her to his side.

“About us,” replied Wayne, truthfully.

And about the e-mails and the rumours. Seroquel had always been a product with a deep, dark secret, one that threatened bring down the whole AZ empire. Everyone who was anyone at AZ knew that, but now the smoke was blowing away and the mirrors were tarnishing. And the execs were looking for people to blame…

“Do you love me?” asked Redacted.

Wayne slid his hand inside her bathrobe. “Of course I do,” he smiled.

And it was true. He loved all of his ladies. Every one of them.

Her bathrobe slid to the floor. Redacted shivered with excitement as Wayne pressed his lips to her (continued next post…)


Well, it could have been like that. Check out Jim Edwards at BNET for the full, hilariously sleazy story from the real world…


Monday, September 25, 2006

Parexel - TGN1412: the TV programme


On UK Channel 4, this Thursday 9pm UK time.

Wednesday, August 02, 2006

TGN 1412 drug trial - the awful aftermath


The Daily Telegraph reports on long-term consequences in some of the TGN1412 victims:

Last week Mr Day passed on a medical assessment by the immunologist Prof Richard Powell to his clients, who include Nav Modi, 24, from Forest Gate, east London, and three other men aged 19, 30 and 29.

Prof Powell wrote of patient A, the 30-year-old: “It is highly likely (more than 50 per cent) that A will develop auto-immune diseases and has definite early signs that a lymphoid malignancy is developing.”

The man, who has not been named, is to meet doctors in the next few weeks to decide on a course of treatment. There is optimism about his chances of survival if it is dealt with at an early stage.

TeGenero has already gone bust. And Parexel dont look to happy either!

Hat tip: Black Triangle

Monday, March 27, 2006

TGN1412 - never say never


Thomas Hunig, the German professor who founded the TeGenero company, said he still hoped the drug, TGN1412, could be brought to the market.

He said he was devastated that the six volunteers in the first human clinical trial were taken gravely ill but said that he was "not going to give up".

Professor Hunig (not pictured above) said: "I do hope TGN1412 can come to the market. This tragic incident does not exclude the theoretical application of TGN1412 some time in the future. "

Amazing!

But he does have some insight:

"I don't want to hurt anybody in any way. I don't want to come across as a crazy scientist who wants to save his baby despite the victims he has taken. Definitely not."

Insiders' view: Dr Hunig should be the next human volunteer to have this stuff injected into him. Come on Thomas, lead from the front!

Also, will Parexel want the contract to do the trial again?

Hat tip: In the pipeline