Project Data Sphere aims to liberate clinical trial data sets from industry and academic vaults, in an attempt to catalyze cancer research and discovery.
In the spirit of open collaboration, crowdsourcing and multidisciplinary approaches to disease, Project Data Sphere will make available, for the first time, clinical trial data sets from pharma and academia, to essentially anyone who registers at ProjectDataSphere.org. The project is housed under the auspices of the Life Sciences Consortium (LSC), itself an arm of George H. Bush's CEO Roundtable on Cancer.
Ben Comer
The concept is purposefully simple: biopharmaceutical companies and academic groups provide data sets from past clinical trials, and anyone with an internet connection can go to the website, register, and download the amassed data for their own research. SAS, the business analytics company, is providing the web platform and functionality for Project Data Sphere, pro bono.
"Provided you're not on the criminal register, you'll have access," says Charles Hugh-Jones, a member of the LSC, and chief medical officer at Sanofi US. Access is not dependent on a valid research proposal or academic credential, because "we can't judge whether someone's got the right research proposal [for fighting cancer], and I would challenge any one committee to have broad enough knowledge to say where data could go in the hands of different groups of people."
At launch in late June or early July, Project Data Sphere will likely contain five or six data sets, including data sets provided by Sanofi. Hugh-Jones says four of the top 10 pharmas are currently preparing data contributions. All of the data will come from cancer trials; data sets will include protocols and case report forms, but will be limited to comparator arm data, at first. The decision to use only comparator data, not active trial arm data, is "really about getting over certain hurdles," says Hugh-Jones. "People have to understand how to de-identify data, they have to get used to some of the IP issues, and legal issues related to sharing data." Even so, a collection of comparator arm data open for independent research is unprecedented. "If I could get 100 comparator arm data sets in one area of cancer, or among 10 rare diseases, that's a terrific database" for modeling disease, says Hugh-Jones. Comparator arm data "feels like a safe space to learn how to work together," says Amy Abernathy, director of the Duke Center for Learning Health Care. Duke is a participating member of the LSC.
Project Data Sphere will make clinical trial data sets available to essentially anyone.
Data providers will retain ownership and existing IP, but people using the data can build on it, to produce their own intellectual property. In the second phase of the project, SAS will provide a built-in analytics capability and forum, so data downloaders can run analytics without leaving the Project Data Sphere website, and talk to each other. Hugh-Jones hopes to eventually start having data user conferences, to promote further collaboration.
Finally, Project Data Sphere presents a positive PR play for pharma and academia. Organizations gifting data are prioritizing the discovery of new cancer treatments over business concerns. For academia, it's a shield against the swords clamoring for the release of data generated via tax dollar-funded NIH grants.
Hugh-Jones is confident that others will contribute data after the initial launch. During a panel on collaboration and transparency at the 10th Annual SAS Health Care & Life Sciences Executive Conference last month, a SAS employee in the audience suggested fomenting an Occupy Clinical Trials movement to advocate for greater data transparency. Indeed, it will take many loud voices and a sustained effort to liberate clinical trial data from life sciences organizations. But cancer, directly or indirectly, affects everyone's lives. While incremental progress has been made, people with cancer still have disturbing similar outcomes—in terms of disease progression and death—as they did 30 years ago. Project Data Sphere is a necessary, all-hands-on-deck approach to tackling the disease.
Ben Comer is Pharm Exec's Senior Editor. He can be reached at bcomer@advanstar.com.
FDA Grants Priority Review to Regeneron’s Eylea for Macular Edema Following Retinal Vein Occlusion
April 18th 2025Regulatory action was based on data from the Phase III QUASAR trial, which demonstrated that Eylea HD dosed every eight weeks achieved non-inferior visual acuity outcomes compared to Eylea in patients with macular edema following retinal vein occlusion.
Addressing Disparities in Psoriasis Trials: Takeda's Strategies for Inclusivity in Clinical Research
April 14th 2025LaShell Robinson, Head of Global Feasibility and Trial Equity at Takeda, speaks about the company's strategies to engage patients in underrepresented populations in its phase III psoriasis trials.
New Insights Into T Cell Exhaustion and Inflammation in Long COVID
April 17th 2025Nigel McCracken, chief operating officer, Virax Biolabs, discusses new findings that reveal altered cytokine activity and evidence of T cell exhaustion in long COVID patients, providing deeper insight into post-infection immune disruption.
Key Findings of the NIAGARA and HIMALAYA Trials
November 8th 2024In this episode of the Pharmaceutical Executive podcast, Shubh Goel, head of immuno-oncology, gastrointestinal tumors, US oncology business unit, AstraZeneca, discusses the findings of the NIAGARA trial in bladder cancer and the significance of the five-year overall survival data from the HIMALAYA trial, particularly the long-term efficacy of the STRIDE regimen for unresectable liver cancer.
Amgen’s Imdelltra Demonstrates Significant Overall Survival Improvement in Small Cell Lung Cancer
April 16th 2025In the Phase III DeLLphi-304 trial, patients with small cell lung cancer administered Imdelltra achieved a statistically significant and clinically meaningful improvement in overall survival compared to standard-of-care chemotherapy.