The Bio Report

Despite the market success of GLP-1 agonists to treat obesity, many patients suffer side effects such as nausea, diarrhea, and vomiting. These medicines also cause significant loss of muscle mass. And when someone discontinues use, they often regain the weight they lost. Skye Bioscience is developing nimacimab, an experimental therapy that has the potential to induce weight loss by inhibiting the CB1 receptor. Because of its different target, it may be able to be used in conjunction with GLP-1 agonists and lower the dose of those drugs to make them more tolerable, or combined with other therapeutic approaches. We spoke to Punit Dhillon, president and CEO of Skye Bioscience, about CB1 as a target for treating obesity, its experimental therapy nimacimab, and the potential to combine it with GLP-1 agonists and other therapeutic approaches.

Many companies are seeking to develop non-opioid treatments for pain, but Persica Pharmaceuticals may be taking a surprising approach for chronic low-back pain. The company’s lead experimental therapy for the condition is an antibiotic. That may sound odd, but it turns out that about half of chronic low back pain cases are due to bacterial infections that occur after herniation of the spinal disc or injury. We spoke to Steve Ruston, CEO of Persica Pharmaceuticals, about the need for new approaches to chronic low back pain, the company’s experimental targeted intradiscal antibiotic injections, and the need to educate physicians about the role infection can play in the condition.

Though there are plenty of therapeutic alternatives for asthma and chronic obstructive pulmonary disease, or COPD, there are no approved biologics for treating acute exacerbations of these conditions. Connect Biopharma believes that’s an opportunity. It's experimental therapy rademikibart has shown promise treating exacerbations and providing sustained improvements. We spoke to Barry Quart, CEO of Connect Biopharma, about the unmet need the company is seeking to address, how rademikibart works, and Connect’s repositioning as a U.S.-centric company.

When Vanderbilt University Medical Center began to consider how big data and precision medicine were going to impact both research and development and clinical care, it struck on the idea of building a large-scale biobank and tying it to its store of millions of electronic health records. That ultimately led to the founding of Nashville Bioscience, a for-profit subsidiary of the medical center. We spoke to Leeland Ekstrom, co-founder and CEO of NashBio, about the company’s data collection methods, the significance of the alliance it's developed with leading biopharmaceutical companies, and how it's enabling a transformation of drug development with data.

Spirulina, also known as blue-green algae, is edible. It can be engineered to cost-effectively produce biologics that can be taken orally. Though people have long sought to do this, Lumen Bioscience has developed platform technology that solved the various challenges is engineering spirulina to produce medicines. We spoke to Brian Finrow, co-founder and CEO of Lumen, about the company’s platform technology, why it makes possible the pursuit of biologics for indications that were previously not practical, and the potential to make these advanced therapies affordable and accessible in parts of the world where people may not have widely enjoyed their benefits.

Cancer is a global disease, and BeOne Medicines believes it should develop its cancer therapies for global markets. To do so, it’s taking innovative approaches to clinical trials, pricing, and manufacturing to enable it to support patients not only in high-income countries but also in low- and middle-income countries. We spoke to Matt Shaulis, general manager of North America for BeOne Medicines, about the significant global disparities in cancer care, the mission of BeOne Medicines to improve access and affordability to therapies, and the opportunities and challenges of taking a global approach to marketing innovative medicines.

The advent of immunotherapies is transforming cancer care. While early efforts have focused on enabling T cells to attack cancers, Myeloid Therapeutics is developing next-generation immunotherapies that use mRNA to train myeloid cells to attack cancer. We spoke to Daniel Getts, founder and CEO of Myeloid Therapeutics, about the limitations of existing immunotherapies, the role myeloid cells play in the immune system, and the benefits of the company’s therapeutic approach.

Despite having taken steps to prepare for a possible pandemic, the United States fared poorly during the COVID outbreak relative to other developed nations. It also sharpened political divides as conspiracy theories and misinformation spread on social media. In “COVID Wars: America’s Struggle Over Public Health and Personal Freedom,” tech entrepreneur-turned-historian Ronald Gruner takes a deep dive into the public data surrounding the pandemic. We spoke to Gruner about putting the pandemic in historical perspective, what the data showed, and the lessons to be learned.

GLP-1 agonists have been a breakthrough for the treatment of obesity, a global problem with serious health risks. While the benefits of these therapies are seen as outweighing the risks, there have been some concerns about the loss of muscle mass, particularly in older people using these drugs. iBio is developing next-generation obesity therapies that may be able to be used in combination with GLP-1 agonists or by themselves. Its lead experimental therapy is a myostatin inhibitor, part of a class of therapies that have been of interest to treat muscle wasting. We spoke to Martin Brenner, CEO and chief scientific officer of iBIO, about obesity, the limits of GLP-1 agonists, and the potential for myostatin inhibitors alone or in combination with GLP-1 agonists.

At the end of 2024, the Advanced Research Projects Agency for Health awarded a team led by the University of Colorado Anschutz Medical Campus, and including the Foundation Fighting Blindness and six other research groups, up to $46 million to advance research to enable human eye transplants to restore vision in people who are blind. The goal of the project is to make whole eye transplantation a reality by 2030. We spoke to Kia Washington, the project’s principal investigator and professor of surgery at the University of Colorado School of Medicine; and Chad Jackson,  senior director of preclinical translational research at the Foundation Fighting Blindness about why no one has been able to restore vision through whole eye transplantation yet, the technological advancements that now put the goal in reach, and why maintaining and restoring the optic nerve remains a central challenge.