Feeds:
Posts
Comments

Last week, I had the pleasure of attending a conference on Emerging Media in Pharma, sponsored by the good folks at CBI. It was held in a Doubletree Hotel in Philly – the majority of pharma-themed conferences are now held in Philly, it seems (with a few scattering into Princeton NJ, or other nearby locales).

My immediate impression was on the downcast side – the number of attendees was clearly going to be small, which can bring a deadening feel to any event. However, on a positive note, a number of my active fellow pharma networkers were there, including Jon Richman, Phil Baumann, and John Mack, and together, we kept up a very lively interaction with the “outside” world that was tuned into to the Twitter #pharmedia hashtag.

This conference had an interesting mix of speakers – the first day was a bit more on the classic principles, case studies, and discussions, but the second day shifted gears into some broader areas, like what the VA is doing to reach suicidal vets, and perspectives from patient advocates (diabetes, in this case). This was helpful because it got us out of the pharma bubble, and into thinking of some other effective networking angles.

Here are some snippets and sound bytes from the tweetstream over the 2 days:

    Years to reach 50 million users: Radio 38 yrs, TV 13 yrs, Facebook 2 yrs

    The “authority shift” on health content – doctor as primary source decreasing, communities/on-line/consumer opinion leaders increasing

    Mobile platforms for patient drug adherence – huge potential. 25% of epharma consumers demand mobile health tracking (among those with mobile)

    Twazzup – very cool context-tracking interface (try it!)

    Strategic changes: 1) push strategies are failing 2) pull strategies are working

    Do pharma marketers really want to start a conversation? Or just talk? And, do consumers want to converse with pharma? It’s not just about pharma talking to consumers and consumers replying. It’s about consumers talking to consumers.

    People here at #pharmedia really want to know HOW to do it. Others are doing it. Here’s all the social media in pharma. http://bit.ly/11dBiH

    AEs (Adverse Events – the reporting of which on-line scares a lot of pharma regulators -SW) are easy to hide behind and help the risk averse. A set process like AE reporting should be easy to overcome.

    Even at this marketing conf. a pharma speaker has to give fair balance and give out the PI. Seriously.

    (Bayer) Connecting patient taking Betaseron with MS-trained nurse and a mentor. Nice. Like the idea of connecting patients with a mentor. If they meet offline, then no off-label or adverse events online.

    Some of ppts are available from #pharmedia as peeps tweet presentations. Wonderful idea! http://tinyurl.com/lnelda @ideahaus My keynote to UCP: Using Social to Grow Social Capital: http://bit.ly/12F0IL

    “If you build it, they will come.” Not. @jonmrich is giving a refresh on web presence, away from static shop front. http://bit.ly/cbidod

    74% of Rx drug WOM takes place in person (less than 10% on-line). Interesting stat from @healthtalker

    “SM is Pharma’s last best hope to improve its image.” Not if it follows this model: http://bit.ly/gwQgO

    Just don’t get the Adverse Event Reporting fear for pharma soc med. Content mgmt, moderation, hand-off to pharmacovigilance. So? The Myth of Adverse Event Reporting. http://bit.ly/JJSl3

    “Twitter is to brains what Google is to servers”

    Personally, if I only hear “rainbows and unicorns” messages about a drug, it definitely raises my eyebrows.

    Victor Wahby, MD going to give an overview of a communications campaign launched by VA (suicide prevention). 3,600 veteran lives (documented) saved from suicide via this campaign?? Wow. The hotline is 800-273-TALK. Here’s a link to a news article about the VA suicide prevention campaign: http://bit.ly/prI2D So often we talk about campaigns and ideas that are abstractions or trivial pursuits. What the VA is doing is life-saving.

    Twegulate! The world’s first FDA-compliance Twitter regulator application for Pharma. ;) (yes, this was a joke mock-up, dreamed up during the prior evening’s tweetup at a local Irish pub) http://bit.ly/CIJUO

    Now, from the patient side: @sixuntilme and @askmanny, two Type 1 diabetics, start with a crucial point. WE ARE PEOPLE. I do wish pharmas would START here when considering Networked Communications: How can we ADD VALUE to our audience?

    askmanny: See the presentation @sixuntilme and I did today: “Become A Partner With The Patient Blogger” http://bit.ly/qJouL

    The “Loads Of Hope” initiative started by P&G teaches a big lesson that all other companies can learn from http://bit.ly/453lq

    Participatory Medicine is being talked about http://e-patients.net being touted. @ePatientDave would be proud.

    Having practiced in US and Asia, I can say participatory medicine is over-rated. Despite my overly participatory style, many patients do best w classic paternalism.

    The Conclusion: If your company can’t be remarkable online, don’t even try. If it’s gonna be overly complicated, forget about it. 

    #Pharmedia was fun, with very active twittering (far more back-channel discussion than in-room, actually!) Thanks to all who took part!

That should give you a pretty good taste of the themes, and the flavor, of the two days.

The organization of the conference was excellent, the food was quite good, and some of us had a very pleasant tweetup with other Philly folks on the Monday evening – which, coincidentally, was being held just a few blocks away. Some speakers bailed at the last minute – that was disruptive – and the use of mics could have been better coordinated. Otherwise, it was a fine time.

Hopefully, I’ll see you at some other upcoming pharma conferences this year – here’s where I’ll be!

JUST IN: Sanofi gets FDA clearance for heart treatment Multaq – The Food and Drug Administration cleared (FDA) Multaq twice-daily 400 mg tablets to reduce the risk of cardiovascular hospitalisation in patients with atrial fibrillation or atrial flutter, Sanofi said on Thursdaymore

More JUST IN: Elan and J&J in a joint venture for Alzheimer’s.

Stiffer warnings (black box) for Chantix and Zyban.

Can I sign up for this trip-to-France-clinical-trial? How about a westbound follow-up to Fiji?

More on the Lantus blow-up this week – reporting rushed because of Sanofi stock drop? FDA raising questions about the scary “conclusions.” And what connections to a competitor does a doctor have who rang the alarm bell?

PLUS: Testing drugs for one thing, finding they work for another.

——

Subscribe to the Impactiviti blog via e-mail

Subscribe to the Impactiviti blog via RSS

Connect with Steve Woodruff

Strangest Indication of the Year Award: first drug I’ve seen with a directional indication – Cephalon, Inc. today announced that it has submitted a supplemental New Drug Application (sNDA) to the U.S. Food and Drug Administration (FDA) requesting approval of NUVIGIL® (armodafinil) Tablets [C-IV] for the indication of improved wakefulness in patients with excessive sleepiness associated with jet lag disorder resulting from eastbound travelmore

Sutent for colon cancer – no dice.

New anemia drug approved – AMAG Pharmaceuticals, Inc. today announced that the U.S. Food and Drug Administration (FDA) has granted marketing approval for Feraheme™ (ferumoxytol) Injection for intravenous (IV) use as an iron replacement therapy for the treatment of iron deficiency anemia in adult patients with chronic kidney disease...more

Cost/benefit ratio of cancer drugs – this is going to be a hot topic in coming years.

Pain drugs under scrutiny.

——

Subscribe to the Impactiviti blog via e-mail

Subscribe to the Impactiviti blog via RSS

Connect with Steve Woodruff

Ouch. Jury returns $ 1.67 billion verdict against Abbott (patent infringement vs J&J) – A U.S. federal jury returned a $1.67 billion verdict against Abbott Laboratories in a patent suit brought by Johnson & Johnson related to arthritis treatments, the drug companies said on Monday. An Abbott spokesman said the company would appeal the verdict delivered in Marshall, Texas. The case involves Humira, Abbott’s newer blockbuster drug that blocks tumor necrosis factor, or TNF, and which competes with Johnson & Johnson’s older blockbuster medication Remicademore

Sanofi hits back on “poor quality” Lantus studies.

Roche leaving PhRMA – Hoffman La Roche is severing its ties to Big Pharma. The venerable drug maker this week plans to drop its membership in the Pharmaceutical Research and Manufacturers Association. PhRMA, as it is known informally, is the leading trade group for the U.S. pharmaceutical industrymore

PLUS – on the far reaches of the cancer treatment galaxy – Australian scientists have developed a “trojan horse” therapy to combat cancer, using a bacterially-derived nano cell to penetrate and disarm the cancer cell before a second nano cell kills it with chemotherapy drugsmore

AND – the doctor will text you now.

——

Subscribe to the Impactiviti blog via e-mail

Subscribe to the Impactiviti blog via RSS

Connect with Steve Woodruff

I think it’s going to be more than 3 today…!

Does Lantus (Sanofi drug for diabetes) increase cancer risk?

Takeda’s alogliptin (new diabetes treatment) – FDA says, more info please.

European Medicines Agency approves a variety pack of new drugs and expanded indications. Here’s the rundown.

Drug companies increasingly using Medical Science liaisons. In my industry crystal ball, I think MSL-type folks will increasingly replace pharma sales reps. More from the original WSJ article here.

Newest version of Elan rumors – Novartis perhaps buying the MS part of the portfolio? Could make sense, given Novartis’ recent entry into that therapeutic area.

Roche: bye-bye Accutane – Roche is pulling its Accutane acne medicine from the U.S. market after juries awarded at least $33 million in damages to users who blamed the drug for bowel disease. Roche notified the U.S. Food and Drug Administration today that it was withdrawing Accutane after a “reevaluation” of its product lines showed it faced serious challenges from generic competitors, company officials said in a statement...more

——

Subscribe to the Impactiviti blog via e-mail

Subscribe to the Impactiviti blog via RSS

Connect with Steve Woodruff

A 9th PML case with Tysabri since reintroduction - Biotechnology company Biogen Idec Inc. said late Friday a ninth Tysabri patient developed a potentially deadly brain infection since the drug was reintroduced to the market in 2006. The drug, which treats multiple sclerosis, was pulled from the market in 2005 following occurrences of a rare, but deadly, brain infection called progressive multifocal leukoencephalopathy. The drug was reintroduced in July of 2006, with restrictions and a monitoring programmore

Merck and Schering-Ploughmore merger info, please (FTC).

Some interesting oncology/HIV links, with hat tip to Sally Church:

:: Glaxo drug delays kidney cancer progression – it will be interesting to see how it compares to, say, Sutent.

:: Perfusion treatment for liver cancer shows some promising results.

:: How does adrenal cancer form?

:: Combined retroviral and targeted chemotherapy treatment may flush out hide-and-seek virus remaining in immune cells.

PLUS – are too many patients self-diagnosing?

——

Subscribe to the Impactiviti blog via e-mail

Subscribe to the Impactiviti blog via RSS

Connect with Steve Woodruff

THE BIG DEAL – Pharma and the U.S. government come up with drug discount agreement. More detail here.

New Forest Labs pneumonia drug reaches goals – Forest Laboratories Inc said on Friday its experimental antibiotic proved to be at least as effective as an older medicine in pneumonia patients, reaching its main goal in two late-stage trials. Forest said its drug, ceftaroline, was well tolerated and met its primary goal of similar effectiveness and high clinical cure rates compared with ceftriaxone in patients with moderate to severe community-acquired, bacterial pneumonia requiring hospitalizationmore

Pfizer manager sentenced for off-label Bextra promotions.

——

Subscribe to the Impactiviti blog via e-mail

Subscribe to the Impactiviti blog via RSS

Connect with Steve Woodruff

I’m prepping to meet tomorrow with a biotech client about potential usage of social media. But in looking over the client’s website, and thinking about pharma SM issues, and reviewing my “Ten Consulting Questions”, I had to chuckle.

We’ll really be brainstorming a communications strategy.

Not a single one of the 10 main issues necessitates social media. It just happens to be a possible tool and approach. As neatly summarized by Geoff Livingston. And encapsulated in this quote from a rather provocative Ad Age article: “What if we stopped getting all hot and heavy over the latest new media success stories du jour, and starting realizing that the real triumph of…a campaign was the product and the story, not the channel used for storytelling?”

I don’t think I ever want to be a “social media guru.” I’d rather become an increasingly effective communications strategist. Who participates in and understands social networking.

We’re better off focusing on terms like community-building, connecting, and communicating. That’s the point. SM tactics are…well, tactics.

UPDATE: The meeting was fantastic…!

Medtronic, a doctor, transparency, and 800K – Remember that former Army doctor accused of faking data in a published study that found positive results for a Medtronic product? Turns out, Medtronic paid him nearly $800,000 over the past three years. Here’s the report from this morning’s WSJmore

RA drug Mabthera: use early, use often – Trials show rituximab, marketed as MabThera, almost completely halts the deterioration of the joints in people showing the first signs of the disease…The latest study on 755 patients shows the drug, when used with the gold standard treatment for early RA methotrexate for a year, not only reduces symptoms but slows joint damage to almost a complete stop if used early enoughmore

Novartis gets approval for…well, you’ll have to read it for yourself. Swiss drugmaker Novartis said Thursday that the U.S. Food and Drug Administration has approved its Ilaris medicine for the treatment of children and adults with cryopyrin-associated periodic syndrome…more

PLUS – Sanofi to donate 100m swine flu vaccines. Nice.

——

Subscribe to the Impactiviti blog via e-mail

Subscribe to the Impactiviti blog via RSS

Connect with Steve Woodruff

Are you trying to find an ideal vendor partner for your sales training or eMarketing endeavors? Contact Impactiviti for expert recommendations…free client consultations!

Why are Doctors so down on Pharma?

Only a tenth of prescriptions are truly “up for grabs”? Interesting analysis – Traditional promotion efforts, including details and sampling, can only affect about 10% of prescriptions, an IMS study found, suggesting that the bulk of promotion dollars is misplacedmore

Another gout drug (this one from Savient Pharmaceuticals) approved by FDA – The 14-to-1 vote for approval reflected a general consensus that the effectiveness of the drug in relieving severe pain and disability outweighed the risk of allergic reactions and suggestions that it could cause cardiovascular problemsmore

PLUS – UCB Pharma comes up with a plan to report Adverse Events via a community site. This is an important initiative – one of the big excuses pharma company regulators have used to shy away from social networking is the AE canard. This issue can be dealt with, and what UCB is doing will help light the way. Plus, here’s a Washington Post article on how drug companies are delving into the on-line space.

Breaking news: Watson acquiring generics maker Arrow.

——

Subscribe to the Impactiviti blog via e-mail

Subscribe to the Impactiviti blog via RSS

Connect with Steve Woodruff

Older Posts »