“Most people have no idea how debilitating iron deficiency anemia can be. As a critical micronutrient, iron has a foundational role to play in multiple biological processes in the body down to the cellular level, its uncorrected deficiency has far-reaching consequences,” says Buddha Chaudhuri, Ph.D., CEO of Biotech company, Keylika. After years working on drug delivery and medical devices, Keylika’s team has pioneered what could be a breakthrough solution: the world’s first buccal (oral) patch for treating iron deficiency.
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When personal health challenges inspire innovation, remarkable solutions can emerge. Such is the story behind NistuHeal, a breakthrough dermocosmetic product addressing eczema and chronic itch. After suffering from relentless eczema for a decade, Buddhadev "Buddha" Chaudhuri, Ph.D. and CEO of Keylika, turned his scientific expertise toward creating a better treatment. What began as a kitchen experiment has evolved into a successful family-run enterprise delivering relief to thousands across India.
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Seaweed might not be the first thing you think of sidling up on a plate with fried eggs and hash browns. But it's high in protein, one of the fastest growing plants on earth, and requires no land, fresh water, or fertilizer.
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Profluent, a biotechnology company that is using AI to design proteins, says it has demonstrated “scaling laws” in the performance of AI models for biology that are similar to those AI researchers have previously claimed for AI models built to handle language.
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GigaCrop was founded by CEO Chris Eiben in 2020 as part of a fellowship with the Berkeley Lab Cyclotron Road program in partnership with non-profit Activate funded by the U.S. DOE., and today (March 11th 2025) they announced $4.5 million of pre-seed round funding led by a venture capital group in California called Playground Global.
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Standout deals include NewLimit’s $72.3 million raise to advance epigenetic rejuvenation and Cyclarity Therapeutics’ $10.3 million round to push forward its senolytic platform. Despite regulatory gray areas and a long road to clinical validation, momentum is building as longevity biotech shifts from speculative science to a potential cornerstone of future healthcare.
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ResVita Bio, a therapeutics company focused on treatments for skin diseases, today announced that the FDA awarded the Orphan Drug Designation to RVB-003 for the treatment of Netherton Syndrome, a chronic and life-threatening skin disorder. This milestone, following the FDAs previous granting of the Rare Pediatric Disease Designation, underscores the impact of ResVita Bio's new platform for continuous protein therapy—a groundbreaking therapeutic approach designed to deliver sustained drug levels directly to the skin, supporting both greater efficacy and improved safety over other topicals.
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Daiichi Sankyo is stepping up its interest in RNA therapies, teaming with Nosis Biosciences to design drug candidates capable of reaching targets beyond the liver.
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Verinomics, a leader in agricultural genomics and gene editing, today unveiled two breakthrough platforms designed to accelerate specialty crop innovation: Genesis™, a transgene-free gene editing platform, primarily for vegetatively propagated crops and Genova™, a genomic-driven breeding acceleration platform for both seed and vegetatively propagated crops. Together, these technologies streamline trait discovery and product development, delivering high-value, market-ready crops faster than ever before.
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Nosis Bio, a startup developing new ways to deliver RNA therapies to specific cells, has struck partnerships with two pharma companies that together could be worth more than $1.5 billion, the company told Endpoints News in an exclusive interview.
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For decades, drug developers have struggled with so-called "undruggable" proteins—those regions of the proteome that evade traditional small molecules and antibodies. But Aikium, led by Eswar Iyer, could be changing the game. In today’s show, Iyer, a prolific scientist with over 100 patents and a background in George Church’s lab, shares how his company is tackling one of the toughest challenges in therapeutics.
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“Many startups have attempted to create new recyclable plastics like we have. But what they have not been able to achieve is creating plastic that is biorenewable and cheaper to recycle,” FutureBio founder Zilong Wang said. “That’s the game-changer.”
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Recently, Cyclarity Therapeutics announced the launch of a Phase 1 human clinical trial for a drug that aims to remove the arterial plaques that lead to heart attacks and strokes.
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In a way, biotech startup Editpep’s story is one faced by many new life sciences companies in a tough funding environment; in a way, too, it is so Berkeley.
Co-founded by University of California, Berkeley postdoctoral researcher looking at ways to cure genetic diseases, an MBA student and a scientific disciple of CRISPR gene-editing technology pioneer Jennifer Doudna, Editpep last month secured an $8.4 million seed financing to take on pediatric brain cancer and other brain diseases.
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Cyclarity Therapeutics is pleased to announce regulatory approval to begin its first-in-human clinical trial. The trial will be conducted at CMAX, one of Australia’s leading clinical research centers, in partnership with Monash University. This effort will be led by Dr. Stephen Nicholls of the Victorian Heart Institute (VHI), a distinguished leader in cardiovascular medicine. In addition to a traditional SAD/MAD phase 1 trial, the authorization includes an allowance to enroll 12 patients with Acute Coronary Syndrome (ACS) to assess the safety of UDP-003 in individuals with plaque buildup, as well as to explore anecdotal evidence of efficacy. This represents a critical first step in evaluating the potential impact of our therapy in a population with high unmet need.
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Happy new year! At Bakar Labs we’re looking forward to a great 2025, starting of course with the JP Morgan Healthcare Conference in SF. Other highlights in the near future: the return of our JETRO entrepreneurs from Japan; the rollout of the Bakar Climate Labs pilot program (look for our web story on Futurebio, our first climate tech tenant); if you’re at the BIO International Convention in Boston, look for our team, we’ll be there. You can count on our September Showcase and our November anniversary party to be bangers. Community is our #1 asset. Thank you for being part of it!
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Amin Zargar literally put skin in his scientific game. Now he hopes to add a deeper layer of funding to his East Bay startup to boost its work on a treatment for a rare and deadly skin disease.
Zargar as a postdoctoral fellow was on an academic track and looking for a job as he stress-tested an idea kicked around with mentor Jay Keasling, a pioneer in synthetic biology at UC Berkeley. What if, they thought, they could genetically engineer a bacteria to convert sugars in skin lotions into therapeutic proteins continuously pumped onto the skin's surface?
In essence, the bacteria would become a 24/7 factory for producing healing proteins.
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