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Newron Reviews FDA Clinical Hold as Phase 3 ENIGMA-TRS Program Advances
Newron Pharmaceuticals has received FDA feedback on a clinical hold at U.S. sites for its Phase 3 ENIGMA-TRS 2 study and is preparing a response while...

Quantum BioPharma Taps Thermo Fisher to Launch Phase 2 Lucid-MS Trial, Advancing Novel Neuroprotective Approach for Multiple Sclerosis
Quantum BioPharma has signed a Study Start-Up Agreement with Thermo Fisher's clinical research business to execute a Phase 2 trial of Lucid-MS, a firs...

Quantum BioPharma Taps Thermo Fisher for Phase 2 Lucid-MS Trial, Advancing Novel Neuroprotective Approach
Quantum BioPharma's agreement with Thermo Fisher's clinical research business moves its lead multiple sclerosis drug Lucid-MS into a phase 2 trial, te...

Quantum BioPharma Partners with Thermo Fisher to Launch Phase 2 Trial of Lucid-MS for Progressive Multiple Sclerosis
Quantum BioPharma has signed a Study Start-Up Agreement with Thermo Fisher Scientific's clinical research business to execute a Phase 2 trial of Lucid...

XORTX Advances XORLO for Gout as FDA Filing Approaches, Targeting Underserved Patient Population
XORTX Therapeutics is advancing XORLO, a proprietary oxypurinol formulation for gout, toward a New Drug Application with the FDA, potentially offering...

Quantum BioPharma Advances Lucid-MS Phase 2 Trial with Thermo Fisher Agreement
Quantum BioPharma's agreement with Thermo Fisher for its Phase 2 Lucid-MS trial marks a critical step toward developing a first-in-class treatment for...

NanoViricides to Present at NIBA 153rd Investment Conference, Highlighting Broad-Spectrum Antiviral Pipeline
NanoViricides will present at the NIBA 153rd Investment Conference on Oct. 7, 2026, showcasing its broad-spectrum antiviral NV-387, which is in Phase ...

Quantum BioPharma Kicks Off Phase 2 Multiple Sclerosis Trial with Thermo Fisher
Quantum BioPharma's Study Start-Up Agreement with Thermo Fisher for its Phase 2 Lucid-MS trial signals a critical step toward developing a first-in-cl...

Okogen Wins CDSCO Authorization for EMERALD Phase 1/2 Study of Treyegen for Acute Infectious Conjunctivitis
India's drug regulator has cleared Okogen's Phase 1/2 EMERALD study of Treyegen, a single therapy targeting both viral and bacterial conjunctivitis, p...

NanoViricides Advances Oral Ebola Treatment NV-387 into Phase II Trial
NanoViricides has provided an update on its Phase II clinical trial of NV-387 Oral Gummies for Ebola, highlighting the potential of an oral antiviral ...

Nutriband Marks Five Years on Nasdaq with Shareholder Letter Outlining AVERSA Fentanyl Progress
Nutriband Inc. celebrates its fifth anniversary on the Nasdaq Capital Market with a shareholder letter detailing the advancement of its abuse-deterren...

Physician Urges Same-Shift MAT Talks in Rural Emergency Departments
Gianluca Cerri, MD, is advocating for a personal policy that ensures every opioid use disorder patient in a rural emergency department receives a same...

Stonegate Updates Coverage on Incannex Healthcare as DReAMzz Trial Advances
Stonegate Capital Partners' updated coverage highlights Incannex Healthcare's progress in clinical execution and the implications for its lead asset I...

New Medical Thriller Exposes Clinical Trial Integrity Crisis
AAG Zacheriel's debut novel, The Vena Protocol: First Blood, uses fiction to spotlight the critical issue of clinical trial data integrity and its imp...

Quantum BioPharma Advances Lucid-MS to Phase 2 Trial for Multiple Sclerosis, Highlights unbuzzd(TM) Royalty Stream
Quantum BioPharma's Lucid-MS is entering a Phase 2 trial in multiple sclerosis patients, while the company also holds a 20% stake and a 7% royalty str...

Quantum BioPharma Advances Lucid-MS to Phase 2 Trial, Highlights Royalty Potential of unbuzzd(TM)
Quantum BioPharma's Lucid-MS multiple sclerosis drug advances to Phase 2 testing while its alcohol metabolism product unbuzzd(TM) offers a 7% royalty ...

Survey Finds Most US Adults Support Vaccines, But Uncertainty Limits Uptake
A new NFID survey reveals that while 77% of US adults support vaccines, only 48% got vaccinated against respiratory diseases in the past year, highlig...

NanoViricides Advances NV-387 Phase II Trials for Mpox and Ebola, Reports Fiscal 2026 Results
NanoViricides, Inc. (NYSE American: NNVC) has received regulatory approval to begin Phase II trials of NV-387 Oral Gummies for Mpox and Ebola in the D...

NanoViricides Launches Phase II Ebola Trial, Testing Oral NV-387 Gummies in DRC
NanoViricides has begun patient enrollment and dosing in a Phase II trial of NV-387 Oral Gummies for Bundibugyo Ebolavirus in the Democratic Republic ...

Quantum BioPharma's FDA Nod for Lucid-MS Phase 2 Testing Signals New Hope for Multiple Sclerosis Patients
Quantum BioPharma's FDA IND approval for Lucid-MS marks a pivotal step toward a phase 2 trial of a novel multiple sclerosis treatment with a unique me...

Nutriband Appoints Former Navy SEAL Robert J. O’Neill to Advisory Board
Nutriband Inc. has appointed former Navy SEAL Robert J. O’Neill to its Advisory Board to help advance its abuse-deterrent transdermal products, includ...

Creative Biolabs Launches Integrated Antibody Engineering Services to Streamline Preclinical Development
Creative Biolabs has introduced a three-part antibody engineering framework to help biopharmaceutical researchers overcome immunogenicity, efficacy, a...

FamiCord AG Signs CDMO Manufacturing Agreement with VERIGRAFT for Pivotal Phase II/III Trial
FamiCord AG's CDMO division Bramble Bio will establish GMP manufacturing for VERIGRAFT's personalized tissue-engineered vein P-TEV in an 18-month deal...

FDA IND Approval Paves Way for Quantum BioPharma's Lucid-MS Phase 2 Trial in Multiple Sclerosis
Quantum BioPharma (NASDAQ: QNTM) has received FDA approval of its IND application for Lucid-MS, enabling phase 2 clinical testing of a novel multiple ...

Annovis Bio Taps Weave AI for Buntanetap NDA Preparation as Phase 3 Data Looms
Annovis Bio's collaboration with Weave Bio to use AI for drafting its buntanetap NDA could speed regulatory submission and strengthen its position in ...

American Heart Association Honors Dr. Katherine R. Tuttle with 2026 Clinical Research Prize for Transforming Kidney and Cardiovascular Care
The American Heart Association will award its 2026 Clinical Research Prize to Dr. Katherine R. Tuttle for her pioneering research that has fundamental...

Boston BioLife's 11-Year Mission Expands with Landmark Translational Longevity Summit
Boston BioLife marks 11 years of bridging science and clinical medicine by co-presenting the Translational Longevity Summit, aiming to accelerate resp...

Tonix Pharmaceuticals Expands TONMYA Medicare Coverage to 32 Million Lives, Bolstering Commercial Reach
Tonix Pharmaceuticals' second major managed Medicare agreement for TONMYA adds approximately 21 million covered lives, bringing total Medicare coverag...

In Vitro ADME Studies Streamline Drug Development with Early Data
In vitro ADME studies provide critical early insights into drug candidates' behavior, reducing costly late-stage failures and accelerating development...

Bacterial Strains Determine Severity of Air Pollution-Linked Infections, Study Finds
A new study reveals that the risk of sepsis, meningitis, and pneumonia from air pollution depends on individual bacterial strains, highlighting the ne...

Peptide Wholesale Supply Expands HPLC Batch Traceability to Bulk Semaglutide and Tirzepatide Orders
Peptide Wholesale Supply now provides HPLC chromatographic data for each batch of BPC-157, Semaglutide, and Tirzepatide bulk orders, enhancing analyti...

Early Clinical Trial Discussions Offer New Hope for Small Cell Lung Cancer Patients
Experts urge small cell lung cancer patients to ask about clinical trials at their first appointment, as emerging research expands treatment options a...

GeoVax and CEPI Partner to Independently Evaluate GEO-MVA in Phase 3 Trial, Aiming to Diversify Global Mpox Vaccine Supply
GeoVax's agreement with CEPI to use its Centralised Laboratory Network for independent testing of GEO-MVA could accelerate the vaccine's development a...

Creative Biolabs Expands Functionalized Lipid Delivery to Overcome Key Research Barriers
Creative Biolabs has expanded its functionalized lipid-based delivery system development to help researchers address stability, targeting, and control...

BioCorRx Adds Former White House Drug Policy Chief to Advisory Board to Advance Addiction Treatment Strategy
BioCorRx Inc. appointed Richard J. Baum, former Acting Director of the White House Office of National Drug Control Policy, to its Strategic Advisory B...

Engineered Suppressor tRNAs Show Promise for Duchenne Muscular Dystrophy, With Broader Implications for Genetic Diseases
Preclinical research published in Science Advances demonstrates that engineered suppressor tRNAs can restore full-length dystrophin and improve muscle...

Regentis Biomaterials Advances GelrinC Pivotal Trial and European Commercialization Plans
Regentis Biomaterials reported first-half 2026 results, highlighting progress in its Phase III GelrinC trial, expanded clinical networks, and a new ma...

Quantum BioPharma's Lucid-MS Enters Phase 2 Trial, Targeting Myelin Repair in Multiple Sclerosis
Quantum BioPharma's Lucid-MS, a first-in-class myelin-protecting drug, receives FDA clearance for a Phase 2 trial in multiple sclerosis, potentially o...

Regentis Biomaterials Advances GelrinC as Potential New Approach to Knee Cartilage Repair
Regentis Biomaterials is developing GelrinC, an off-the-shelf hydrogel implant designed to regenerate knee cartilage, which could significantly improv...

VERAXA Biotech Appoints Dr. Christoph Erkel as CSO to Steer BiTAC® Toward Clinical Development
VERAXA Biotech's appointment of Dr. Christoph Erkel as chief scientific officer signals a strategic push to advance its BiTAC® T-cell engager and broa...

Quantum BioPharma Advances Lucid-MS Toward Phase 2 Trial Following FDA Clearance
Quantum BioPharma's Lucid-MS, a first-in-class non-covalent PAD2 inhibitor, is advancing to a Phase 2 trial for multiple sclerosis after FDA clearance...

FDA Clearance of Quantum BioPharma's Lucid-MS Marks Historic First in MS Treatment, Targeting Myelin Repair
Quantum BioPharma receives FDA clearance for the first-ever phase 2 trial of a myelin-rebuilding drug for multiple sclerosis, a potential game-changer...

FDA Greenlights First-in-Human Trial of Myelin-Rebuilding MS Drug, Signaling Potential Shift in Multibillion-Dollar Market
Quantum BioPharma's FDA clearance to test Lucid-MS, a first-in-class multiple sclerosis drug designed to shield and rebuild myelin, marks a historic d...

Helus Pharma CEO to Present at Morgan Stanley Healthcare Conference, Spotlighting Phase 3 Depression Program
Helus Pharma's CEO will participate in a fireside chat at the Morgan Stanley Global Healthcare Conference, providing a platform to highlight the compa...

Onco-Innovations CMO Highlights Novel PNKP-Targeting Cancer Drug ONC010 in BioMedWire Podcast
Onco-Innovations' CMO discussed the company's lead drug candidate ONC010, which targets PNKP and uses two selectivity mechanisms, and its potential to...

Quantum BioPharma's Lucid-MS Gains FDA Clearance for Phase 2 Multiple Sclerosis Trial
Quantum BioPharma's FDA clearance to begin a Phase 2 trial of Lucid-MS, a first-in-class non-covalent PAD2 inhibitor, positions the company to potenti...


