Some talks in the US and Canada. COME!

January 30th, 2013 by Ben Goldacre in bad science | 2 Comments »

Bad Pharma is out in the US and Canada on 5th Feb, which is extremely good news (sorry about the delay, floods and hurricanes apparently..). I’ll be doing a few public lectures in various places, alongside media stuff and other things, there’s a list of open ones below.

If you’re a US podcaster or blogger and you want to chat about bad behaviour in the pharma industry then do please email the three of us (Brian.Gittis@fsgbooks.com ben@badscience.net zross@unitedagents.co.uk).

Also: in the UK I’ve done a gazillion talks, and the most fun things always come from random people. So if from the list below it looks like I’m passing through your town and you want me to do a talk in your university, a pub, or an event, or you think there’s someone I should meet, a campaigner, an academic, a journalist, then please contact jglover@randomhouse.com for Canada, and Brian.Gittis@fsgbooks.com for the US. Do also cc me, ben@badscience.net, and we’ll try to fit it in around the various bits of other work while I’m out there.

Cheers!

badpharmaUS

You can buy the US edition of Bad Pharma here.

PORTLAND, OR
Sun 17th Feb 7:30pm
Powell’s Bookstore, 1005 West Burnside.
Talk, Q&A, and signing

www.powells.com/locations/powells-city-of-books/

 

SEATTLE, WA
Mon 18th Feb 7:30pm
Town Hall, downstairs, enter on Seneca Street
Talk, Q&A, and signing:

townhallseattle.org/ben-goldacre-how-drug-companies-mislead-doctors-harm-patients/

 

NEW YORK CITY, NY
Thurs 21st Feb 7:00pm
Talk, Q&A, and signing
NYC Skeptics at University Settlement, 184 Eldridge Street

nycskeptics.org/events/rationally-speaking-podcast-live-with-guest-ben-goldacre.html

 

TORONTO, CANADA
Friday, 15th Feb, 7:30pm
Massey College lecture, free and open to the public.

www.masseycollege.ca

Thursday 14th Feb, 6pm-8pm
Pub talk organised by @julia, free, open to all

www.supermarkettoronto.com/

 

www.ted.com/talks/ben_goldacre_battling_bad_science.html

AllTrials campaign launches, please sign and spread!

January 16th, 2013 by Ben Goldacre in alltrials campaign, big pharma, publication bias | 2 Comments »

I am very pleased to announce the launch of a prominent campaign for access to all trial results, which we have launched this week at www.alltrials.net, with myself, Sense About Science, Sir Iain Chalmers from the James Lind Initiative (previously co-founder of Cochrane), Dr Fiona Godlee (Editor in Chief of the BMJ), and Dr Carl Heneghan (Director of the Centre for Evidence Based Medicine at Oxford).

The response so far, in a very short period of time, has been phenomenal. We have collected over 7,000 signatures already, simply from tweeting, and several extremely high profile organisations have signed up already, including: Read the rest of this entry »

Health Select Committee call on NICE, GMC, pharma industry to address missing data

January 16th, 2013 by Ben Goldacre in bad science | 4 Comments »

Excellent to see the UK House Of Commons Health Select Committee making such a clear statement about the ongoing problem of missing trial results, which the ABPI have laughably claimed is “historic“.

They call upon NICE, the GMC and the pharmaceutical industry to address the problem, and they also take a very strong clear position: that withholding the results of clinical trials should be neither legal nor ethical.   Read the rest of this entry »

I made this Radio 4 documentary on randomised trials on government policy

January 6th, 2013 by Ben Goldacre in bad science, evidence based policy, government reports, podcast, politics | 4 Comments »

Here’s a documentary I made for BBC Radio 4 (with producer Rami Tzabar) about evidence based social policy, and why we should do more randomised trials in government. It’s good fun, 40 minutes, with contributions from Dean Karlan (who wrote this book and is behind all these excellent trials on reducing poverty), Prof Sheila Bird, Jonathan Portes from NIESR (his excellent blog here), the man they call GOD, and many more.

www.bbc.co.uk/programmes/b01phhb9

It’s also Radio 4 documentary of the week (woo!) which means you can download it as an mp3. The link is live for another 5 days, and it works for some countries outside the UK too.

www.bbc.co.uk/podcasts/series/r4choice

And now that it’s expired on iPlayer, you can listen to it on FigShare here:

figshare.com/articles/R4Doc_04_Jan_13_Ben_Goldacre/105918

If you’re interested in reading more evidence based policy, I highly recommend this Cabinet Office paper that I co-authored a few months ago, downloadable for free online. As explained here, it’s brief, and very much designed to be the Ladybird Book of RCTs in Government. If you want more on the uses for randomised trials in criminal justice, I wrote this in the British Medical Journal with Sheila Bird and John Strang in 2011 (sorry it’s not open access, I’ll try to fix that soon). More to come on this topic soon. Read the rest of this entry »

Interview on missing trials with the Institute for Clinical Research

December 22nd, 2012 by Ben Goldacre in bad science | 7 Comments »

Just catching up on posting some overdue entries, I’ll do a roundup of progress on the hidden trial data problem in a while. Firstly, briefly, here’s an interview I did with the members’ journal of the Institute for Clinical Research (the people who design and run clinical trials). It’s a good, constructive discussion, mostly covering publication bias and missing data. Shortly afterwards, the ICR issued a position statement on transparency and hidden data, which is (partially!) good.   Read the rest of this entry »

MPs write to Public Accounts Committee to request action on hidden trials and Tamiflu.

December 14th, 2012 by Ben Goldacre in ABPI, alltrials campaign | 8 Comments »

The letter below has been sent to Margaret Hodge, Chair of the Public Accounts Committee, asking her to take action on the ongoing problem of hidden trials, and specifically Tamiflu.

The very notion that we spent £500 million on Tamiflu – with information about over half of the clinical trials still being withheld – is nothing short of absurd. For context, £500 million is 5% of the total NHS drugs budget (£10 billion) for one year. This ongoing issue of secrecy around clinical trials wastes money and harms patients, and it has persisted for several reasons. Read the rest of this entry »

False claims by Stephen Whitehead and Deepak Khanna of the ABPI

December 14th, 2012 by Ben Goldacre in ABPI, bad science, Stephen Whitehead | 4 Comments »

Briefly: the ABPI have engaged in an energetic personal smear campaign, as predicted at the end of Bad Pharma. I’ll think about posting the details from leaked and external ABPI documents at some stage. I’m posting some correspondence today because the CEO and President of the ABPI have both falsely claimed to MPs and journalists that I’ve refused to meet them over many years. This is silly and untrue, especially when the ABPI have also specifically stated in public that they are refusing to engage with my concerns. Both Stephen Whitehead (CEO) and Deepak Khanna (President) have failed to provide any explanation of why they’ve made these false claims, or give a full list of the people they’ve misled, so regrettably I’m posting my letter to them here. Read the rest of this entry »

Win. Parliamentary Sci Tech Committee announces official inquiry into missing trial data.

December 13th, 2012 by Ben Goldacre in bad science | 2 Comments »

Sorry to have been absent, I’ve been working away on several projects behind the scenes, on which much (much!) more shortly.

I’m extremely pleased to say that the Commons Science and Technology Select Committee have just announced that they will now conduct a formal inquiry into missing trial data. Full details are posted below, and a briefing on the basics of this ongoing problem can be found at the bottom of this post.

I will post more on this, and the wider campaign, shortly, but before I run to a meeting, I should tell you one story that explains why I think this inquiry is important.

Two weeks ago the European Medicines Agency held a meeting on transparency and clinical trials (I was on the panel). During the discussion, a lawyer working for a drug company stood up and said, quite simply: we pay for this data to be collected, we should be able to control how it is used. There was no sharp intake of breath at this comment, in a room full of 200 regulators, researchers, industry representatives, and doctors.

To me, this shows that we have become detached from reality, through the abstractions of evidence, and how we have failed to focus on the needs of patients. It is one thing to talk about controlling data in technical meetings. But I doubt any one of the people responsible for creating and perpetuating a situation where trial data is routinely withheld could walk up to a patient and say: “we think we should be allowed to withhold vital evidence about whether that pill works or not, from you, the person swallowing it.”

That’s why I think this inquiry is potentially very important. This problem has persisted, because lot of people – some of them in positions of great responsibility, as we shall see – have worked very hard to shut down any legitimate public discussion of its existence.

I think transparency is a win for academia, and for industry. I also think, with the rise of open data and transparency in government and elsewhere, it’s an inevitability. So I’m sad to see them resisting it so aggressively, and I hope they can change.

www.parliament.uk/business/committees/committees-a-z/commons-select/science-and-technology-committee/news/121213-clinical-trials-inquiry-announced/

Committee to inquire into clinical trials and disclosure of data

13 December 2012

Clinical trials in the UK are regulated by the Clinical Trials Directive which was transposed into UK law by the Medicines for Human Use (Clinical Trials) Regulations 2004. In December 2011, the Health Research Authority was created to protect and promote the interests of patients and the public in health research. In July 2012, the European Commission produced proposals to revise the Clinical Trials Directive.
Transparency and disclosure of clinical trial data have been topical recently, in part due to the recently published book Bad Pharma, by Dr Ben Goldacre. It highlighted that pharmaceutical companies are entitled to conduct numerous clinical trials on a new drug but publish selectively, thus skewing the evidence base available for doctors and patients seeking to make informed decisions.

 

Terms of Reference

The Committee seeks written submissions on the following matters:
1. Do the European Commission’s proposed revisions to the Clinical Trials Directive address the main barriers to conducting clinical trials in the UK and EU?
2. What is the role of the Health Research Authority (HRA) in relation to clinical trials and how effective has it been to date?
3. What evidence is there that pharmaceutical companies withhold clinical trial data and what impact does this have on public health?
4. How could the occurrence and results of clinical trials be made more open to scrutiny? Who should be responsible?
5. Can lessons about transparency and disclosure of clinical data be learned from other countries?

Submitting written evidence
As part of a scheme to promote paperless working and maximise efficiency, the Committee is encouraging written submissions for this inquiry to be sent by email to scitechcom@parliament.uk and marked ‘Clinical Trials’.

The Committee invites written submissions on these issues by noon on Friday 22 February 2013.

Each submission should:
a) be no more than 3,000 words in length
b) be in Word format with as little use of colour or logos as possible
c) have numbered paragraphs
d) include a declaration of interests.

If you need to send a paper copy please send it to:
The Clerk
Science and Technology Committee
House of Commons
7 Millbank
London SW1P 3JA
Please note that:

• Material already published elsewhere should not form the basis of a submission, but may be referred to within a proposed memorandum, in which case a hard copy of the published work should be included.
• Memoranda submitted must be kept confidential until published by the Committee, unless publication by the person or organisation submitting it is specifically authorised.
• Once submitted, evidence is the property of the Committee. The Committee normally, though not always, chooses to make public the written evidence it receives, by publishing it on the internet (where it will be searchable), by printing it or by making it available through the Parliamentary Archives. If there is any information you believe to be sensitive you should highlight it and explain what harm you believe would result from its disclosure. The Committee will take this into account in deciding whether to publish or further disclose the evidence.
• Select Committees are unable to investigate individual cases.
More information on submitting evidence to Select Committees may be found on the parliamentary website at:www.parliament.uk/get-involved/have-your-say/take-part-in-committee-inquiries/witness/

 

FURTHER INFORMATION

Committee Membership:
Andrew Miller (Labour, Ellesmere Port and Neston) (Chair)
Caroline Dinenage (Conservative, Gosport)
Jim Dowd (Labour, Lewisham West and Penge)
Stephen Metcalfe (Conservative, South Basildon and East Thurrock)
David Morris (Conservative, Morecambe and Lunesdale)
Stephen Mosley (Conservative, City of Chester)
Pamela Nash (Labour, Airdrie and Shotts)
Sarah Newton (Conservative, Truro and Falmouth)
Graham Stringer (Labour, Blackley and Broughton)
Hywel Williams (Plaid Cymru, Arfon)
Roger Williams (Liberal Democrat, Brecon and Radnorshire)
Specific Committee information:  scitechcom@parliament.uk / 020 7219 2793
Media information: Nick Davies  daviesnick@parliament.uk / 020 7219 3297
Committee website: www.parliament.uk/science
Watch committees and parliamentary debates online: www.parliamentlive.tv
Publications / Reports / Reference Material: Copies of all select committee reports are available from the Parliamentary Bookshop (12 Bridge St, Westminster, 020 7219 3890) or the Stationery Office (0845 7023474).  Committee reports, press releases, evidence transcripts, Bills; research papers, a directory of MPs, plus Hansard (from 8am daily) and much more, can be found onwww.parliament.uk.

Questions in Parliament, and a briefing note on missing trials: updated.

October 23rd, 2012 by Ben Goldacre in big pharma, hiding data, publication bias | 4 Comments »

This morning at 11:30, Dr Sarah Wollaston MP will ask questions in parliament about the ongoing scandal of missing trial data. This is widely recognised as a problem by academics and doctors, but governments, regulators, and journalists have neglected the problem, while industry simply denies it. Watch the questions live here or watch it later here.

As an example, we spent £500m stockpiling Tamiflu in the UK, but the company Roche are still withholding vitally important information about the trials on whether it works from Cochrane, the international academic collaboration who make gold standard reviews of evidence for doctors, patients, and governments.

Apparently this morning the Department of Health issued a statement to the Today Programme stating that all data from all trials on all drugs is already available by law. This is not true: but there may have been a communication problem, I am hoping to obtain a copy of this statement, and if you have one, please send it to ben@badscience.net

Here are two articles from the Times today, on this issue. The first is a comment piece (by me). The second is a news piece about the growing number of doctors and academics speaking out on this issue, including editors of major journals, founders and directors of Cochrane, senior medics and academics, etc.  Read the rest of this entry »

Great article in Trials, on why regulators should stop withholding trial info from doctors and patients

October 18th, 2012 by Ben Goldacre in bad science, big pharma | 5 Comments »

One thing in Bad Pharma has shocked readers more than anything else: the way that vitally important information about trials is withheld from doctors and patients, not just by drug companies, but also by government bodies such NICE and the European Medicines Agency (the body that approves and regulates medicines for the UK).

Read the rest of this entry »