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Robin Forrest Profile
Robin Forrest

@robinjforrest_

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41

Research Fellow @DeptPopMed / @HarvardMed || PhD candidate @LSEHealthPolicy

London, England
Joined January 2018
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@robinjforrest_
Robin Forrest
1 year
New paper in @TheLancetOncol. We explore the extent to which individuals could be willing to wait in exchange for greater certainty of the survival benefit of new cancer drugs. Thanks to co-auths: @mylene_lagarde, @AggarwalOnc, & Huseyin Naci. đź”— https://t.co/lw3KPBTcZy
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thelancet.com
Many cancer drugs approved through the FDA's accelerated approval pathway do not offer any survival benefit to patients. In this study, individuals expressed strong preferences for certainty that a...
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@robinjforrest_
Robin Forrest
9 months
Interesting piece from @VPrasadMDMPH on surrogate endpoints and their (potential) impact on efficiency and the cancer drug pipeline. Good to see our study discussed in context!
@VPrasadMDMPH
Vinay Prasad MD MPH
9 months
Just out in @NatRevClinOncol my latest on Surrogate Endpoints from the patient's perspective Despite writing on this topic for 15 years, hope to offer new ideas in this piece @vkprasadlab @Sensible__Med @Plenary_Session
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@LSEHealthPolicy
LSE Health Policy
1 year
To what extent would individuals be willing to wait in exchange for greater certainty of the survival benefit of new cancer drugs? New study in @TheLancetOncol by @robinjforrest_, @mylene_lagarde, @AggarwalOnc, & Dr. Huseyin Naci. Read nowđź”— https://t.co/Sd5kU3kMWK
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@oncology_bg
Bishal Gyawali, MD, PhD, FASCO
1 year
A very relevant and meaningful study. Understanding patients’ preferences for speed versus certainty of benefit- the trade-off of accelerated approval.
@SullivanProf
Richard Sullivan
1 year
This is the first solid evidence to show that cancer patients prefer certainty over speed of access to new cancer drugs. This directly challenges the current regulatory ecosystem. @myESMO @ASCO @FDA
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@AdamR_PhD
Adam Raymakers
1 year
Interesting new work from authors @LSEHealthPolicy! 'Although people with experience of cancer place high value on faster access to new drugs, they also place utmost value on high certainty that new cancer drugs will ultimately offer survival benefit.' https://t.co/myGTr7rdQp
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thelancet.com
Many cancer drugs approved through the FDA's accelerated approval pathway do not offer any survival benefit to patients. In this study, individuals expressed strong preferences for certainty that a...
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@kjmeetswrld
Kristina Jenei
1 year
🚨Our article out today in @TheLancetOncol Are countries harmonizing up or down? A 🧵 We examine the clinical benefit, #HTA review times, and prices of drugs reviewed through Project Orbis Cc: @VPrasadMDMPH @agentilini_ @AlysonHaslam
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@LSEHealthPolicy
LSE Health Policy
3 years
In a new @bmj_latest editorial, the department’s @robinjforrest_ and Huseyin Naci discuss how the UK Government can prioritise patients in ongoing negotiations with the pharmaceutical industry over drug pricing. Access full editorial from here: ➡️ https://t.co/31zX5hvxNY
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@bmj_latest
The BMJ
3 years
Every five years or so, an agreement is brokered between the UK government and the drug industry that shapes the pricing and reimbursement landscape for medicines. What do we need to know ahead of negotiations for the next version of the agreement? https://t.co/3FyMOu7r6x
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bmj.com
Overpaying for medicines diverts funds away from other treatments and services For over six decades, an agreement has been brokered every five years or so between the UK government and the drug...
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@JAMAHealthForum
JAMA Health Forum
3 years
Prior authorization requirements for 1/3 of new drugs in Medicare Part D are more restrictive than FDA labeling, according this cross-sectional study. @LSEHealthPolicy @PortalResearch @akesselheim @robinjforrest_
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@HealthFdn
The Health Foundation
3 years
NEW: Our #REALCentre commissioned @LSEHealthPolicy to research pharmaceutical policy in the UK. They identify 🔎 ▶️ shortcomings of current pharmaceutical policy ▶️ key principles for building a more coherent system. Read the final reports 🔽 https://t.co/NHCMebY0ef
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health.org.uk
This project, led by London School of Economics and Political Science, reviewed the literature and relevant data to better understand pharmaceutical policy in the UK.
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@LSEHealthPolicy
LSE Health Policy
3 years
Want to learn more about pharmaceutical policy and economics? In a new report commissioned by @HealthFdn #REAL Centre, the Department’s Huseyin Naci & @robinjforrest_ explain pharmaceutical discovery, development, approval and adoption. ➡️ Access here: https://t.co/194uMOrvhc
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@JAMAHealthForum
JAMA Health Forum
3 years
Prior authorization requirements for 1/3 of new drugs in Medicare Part D are more restrictive than FDA labeling, according this cross-sectional study. @LSEHealthPolicy @PortalResearch @akesselheim @robinjforrest_
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@LSE_US
LSE Phelan US Centre
3 years
Congratulations to our seven PhD Grant Recipients for 2022-23! Read more about our PhD grants scheme 👇 https://t.co/pDsCwPq2iX
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@LSEUSAblog
LSE USAPP blog
3 years
The size of the US pharmaceutical market means that the US Food and Drug Administration has a disproportionately large global influence writes @robinjforrest_ of @LSEHealthPolicy https://t.co/LsaTzQXmk6
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@MichaelMarmot
Sir Michael Marmot
4 years
"If you have to worry about whether you have food for dinner that evening, and for the rent on Friday, you have little space to think about anything else. Such stress can permanently affect the development of your children".
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theguardian.com
Poverty is literally a matter of life and death for those on the margins, and the government has so far failed to step in, says Michael Marmot, director of the UCL Institute of Health Equity
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@robinjforrest_
Robin Forrest
4 years
At the top of my contribution list: focus disproportionately on provision in UK regions with lowest screening uptake and lowest rates of early diagnosis.
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