The ROGUE device is being developed thanks to a $34.9 million grant from ARPA-H.
The rising prominence of GLP-1s and anti-obesity medications is causing the pharmaceutical industry to pay more attention to weight-loss and diabetes treatments.
The Advanced Research Projects Agency for Health (ARPA-H) awarded $34.9 million to Rice University who will, as part of a multi-university research team, develop a bioelectronic implant designed to improve adherence for type 2 diabetes treatment.1 The device is named ROGUE, which stands for Rx On-site Generation Using Electronics. According to a press release from Rice University, the device will house cells that produce T2D and obesity therapies directly in response to the patient’s physiological needs.
In a press release, Rice University professor of bioengineering and faculty director of the Rice Biotech Launch Pad Omid Veiseh said, “ROGUE's innovative design combines efficient biological manufacturing, long-term durability and patient-friendly features that have the potential to transform the landscape of biologics delivery. With the Rice Biotech Launch Pad leading the clinical translation and commercialization efforts, this funding will allow us to expedite the development and clinical trials of this groundbreaking technology, making it accessible to patients sooner."
Executive director of the Rice accelerator Paul Wotton added, “With the Biotech Launch Pad, our goal is venture creation in parallel to the groundbreaking research at Rice and its collaborating institutions. With the Biotech Launch Pad, our goal is venture creation in parallel to the groundbreaking research at Rice and its collaborating institutions. This level of support speaks volumes to just how transformative these innovations could be, and therefore how important it is to facilitate their translation.”
The device is designed to be implanted in the patient and will require weekly recharging from a wearable device. It will be capable of supporting, monitoring, and adjusting drug production and dosing when properly charged.
"I am absolutely thrilled by ARPA-H's strong support for the Rice Biotech Launchpad's efforts in accelerating breakthrough bioelectronic technology transition from the bench to the bedside," said Paul Cherukuri, Rice's vice president for innovation and chief innovation officer.
Carnegie Mellon materials science and bioengineer Tzahi Cohen-Karni added, “Our approach enables on-demand production of therapeutics in a highly energy-efficient manner. This technology not only simplifies the delivery of life-saving medications but also enhances patient comfort and adherence. ROGUE's precision and adaptability offer a much-needed improvement in both treatment efficacy and patient experience."
Jonathan Rivnay, a professor of biomedical engineering at Northwestern University, said, “ROGUE's ability to produce glucagon-like peptide 1 receptor agonist (GLP-1 RA) on site will address these high costs and improve patient adherence by eliminating the need for frequent injections. GLP-1 RAs have proven effective in enhancing insulin secretion, reducing glucose levels and promoting significant weight loss, making them a first-line therapy for diabetes and obesity.”
Rivnay continued, “Our collaborative efforts are paving the way for the ROGUE platform to become a revolutionary force in the field of biologics. This technology not only addresses the limitations of current biologics but also offers a sustainable, long-term solution for managing chronic diseases."
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.
Fake Weight Loss Drugs: Growing Threat to Consumer Health
October 25th 2024In this episode of the Pharmaceutical Executive podcast, UpScriptHealth's Peter Ax, Founder and CEO, and George Jones, Chief Operations Officer, discuss the issue of counterfeit weight loss drugs, the potential health risks associated with them, increasing access to legitimate weight loss medications and more.
Johnson & Johnson Seeks FDA Approval for Subcutaneous Tremfya Regimen for Ulcerative Colitis
November 22nd 2024Johnson & Johnson has submitted a supplemental Biologics License Application to the FDA for a subcutaneous induction regimen of Tremfya for adults with moderately to severely active ulcerative colitis based on positive Phase III ASTRO trial results.