Changeflow GovPing Healthcare & Life Sciences

Drug approvals, medical device recalls, clinical trial registrations, hospital licensing actions, healthcare M&A, HIPAA enforcement, CMS reimbursement rules, and the patent filings behind tomorrow's therapies. The Healthcare and Life Sciences hub pulls from 374 official sources spanning the FDA, EMA, MHRA, CMS, NIH, HHS-OIG, state health departments, state pharmacy boards, USPTO, and EPO.

Around 6,500 new entries a month, the highest-volume sector GovPing covers. Coverage includes Phase 1-4 clinical trial postings, novel drug approvals, biosimilar guidance, Class I-III device recalls, warning letters to manufacturers, advisory committee meeting notices, state medical board disciplinary actions, hospital JCAHO accreditation events, and the CMS rulemaking that drives reimbursement.

Watch this hub if you scout drug pipeline opportunities, run regulatory affairs at a sponsor, advise hospital systems on compliance, follow biotech equity research, or compete in surgical robotics and diagnostic imaging. Every entry carries a verbatim quote, a timestamp, and a stable URL back to the original FDA, EMA, or other source.

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Deuterated selenophenochromenes for cancer treatment, Latvian Institute

Deuterated selenophenochromenes for cancer treatment, Latvian Institute

Routine Notice
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Aryl Glucoside SGLT1 Inhibitor Patent, Shanghai Zheye

Aryl Glucoside SGLT1 Inhibitor Patent, Shanghai Zheye

Routine Notice
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Crystalline heterocyclic compound patent granted to JW Pharmaceutical

Crystalline heterocyclic compound patent granted to JW Pharmaceutical

Routine Notice
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US12612427B2 - SGLT1 Inhibitor Patent to Shanghai Zheye Biotechnology

USPTO granted Patent US12612427B2 to Shanghai Zheye Biotechnology Co. Ltd. on April 28, 2026, covering an aryl glucoside derivative that inhibits sodium-glucose co-transporter 1 (SGLT1). The patented compound and pharmaceutical compositions may be used for treating diabetes, cardiovascular and cerebrovascular diseases, weight loss, fatty liver disease, constipation, metabolism-related diseases, and tumor treatment. The patent application was filed November 24, 2020 (Application No. 18023883) and contains 14 claims.

Routine Rule Intellectual Property
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Triazolopyridine Thiophene Carboxamides for Neurodegenerative Diseases

Triazolopyridine Thiophene Carboxamides for Neurodegenerative Diseases

Routine Notice
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2028 Medicaid HCBS Quality Measure Set, Comment Deadline May 28

CMS is seeking public comment on the 2028 HCBS Quality Measure Set, which establishes nationally standardized quality measures for Medicaid-funded home and community-based services. The notice proposes 23 mandatory measures including experience of care surveys, assessment measures, and administrative data measures, plus voluntary measures (LTSS-4 and MLTSS-5). States would be required to report 9-19 mandatory measures depending on populations served and surveys selected. Stratified data reporting by geography would be phased in at 25% by July 9, 2028, 50% by July 9, 2030, and 100% by July 9, 2032. Comments are due May 28, 2026.

Priority review Consultation Healthcare
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BioNTech SE Individualized Cancer Vaccine Patent Granted US12611449B2

BioNTech SE has been granted US Patent 12611449B2 (Kind B2) for individualized cancer vaccines specific to a patient's tumor, based on transcriptome analysis of tumor specimens to identify RNA transcripts excessively upregulated in the patient's cancer cells. The inventors are Ugur Sahin, Mathias Vormehr, and Thomas Bukur. The patent, filed July 23, 2019, contains 8 claims and covers vaccines that induce immune responses against tumor-associated antigens by breaking self-tolerance.

Routine Rule Intellectual Property
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Centessa A1AT Deficiency Treatment Patent US12611402B2

Centessa Pharmaceuticals (UK) Limited has been granted US Patent 12611402B2 for carboxylic acid compounds and pharmaceutical compositions for treating alpha-1 antitrypsin deficiency (A1AT/AATD). The patent, which names Nigel Ramsden, David John Fox, James Andrew Huntington, and James Michael Tomlinson as inventors, was filed on June 13, 2022 and issued April 28, 2026. The patent contains 17 claims covering compounds classified under CPC categories A61K 31/451, A61K 31/4015, and A61K 31/4708.

Routine Rule Intellectual Property
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Tiratricol Drug Compositions for MCT8 Deficiency - US12611383B1

The USPTO granted US Patent 12611383B1 to Rare Thyroid Therapeutics International AB covering pharmaceutical compositions of tiratricol and/or salts thereof for treating MCT8 deficiency. The patent, with 19 claims, names Katayoun Welin-Berger as inventor and was filed on July 7, 2025. Patent grants confer exclusive market rights to the assignee for the claimed compositions and methods of use.

Routine Notice Intellectual Property
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Inhalable Rapamycin PAH Treatment, OrphAI Therapeutics

The USPTO granted Patent US12611398B2 to OrphAI Therapeutics Inc. on April 28, 2026, covering methods and compositions for treating pulmonary arterial hypertension using inhalable rapamycin formulations. The patent application, filed on October 14, 2022 under application number 17965859, contains 36 claims and is classified under CPC codes A61K 31/436, A61K 9/0075, and A61K 9/12. Inventors include Thomas Armer, Lawrence S. Melvin Jr., Jonathan M. Rothberg, and Henri Lichenstein.

Routine Rule Intellectual Property
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Douglas Pharmaceuticals Extended Release Formulation for Treatment-Resistant Depression and Anxiety

The USPTO granted patent US12611386B2 to Douglas Pharmaceuticals Ltd. on April 28, 2026, covering an oral extended release pharmaceutical formulation for treating treatment-resistant depression and treatment-resistant anxiety. The patent (23 claims, CPC classification A61K 31/2031) names Paul William Glue, Natalie June Medlicott, Peter William Surman, and Yuefeng Long as inventors, with a filing date of September 22, 2021 and application number 18028202. Patent grants are final, binding intellectual property rights that give the assignee exclusive rights to the claimed invention.

Routine Notice Intellectual Property
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Recombinant adeno-associated virus vectors to target medullary thyroid carcinoma

The USPTO granted Patent US12611468B2 to the University of Florida Research Foundation, Incorporated on April 28, 2026, covering recombinant adeno-associated virus (rAAV) vectors engineered to target medullary thyroid carcinoma cells. The patent (10 claims) includes mutations in surface-exposed amino acids of the rAAV particle and a truncated calcitonin promoter to enhance transduction of carcinoma cells. The filing date was February 1, 2022, under application number 17590557.

Routine Rule Intellectual Property
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Gilead Sciences HIV-1 Immune Response Patent, Adenovirus Vector and TLR7 Agonist

The USPTO has granted US Patent 12,614,453 B2 to Gilead Sciences, Inc. covering methods of inducing an HIV-1-specific immune response using a chimpanzee adenovirus vector encoding an HIVACAT T-cell immunogen in combination with a TLR7 agonist. The patent also protects compositions and kits for this combination and their use in treating or preventing HIV infection in humans. The patent contains 25 claims and names five inventors: Romas Geleziunas, Devi Sengupta, Christian Brander, Beatriz Mothe Pujadas, and Ian McGowan.

Routine Rule Intellectual Property
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REGENXBIO Granted US12612644B2 for Scalable Recombinant AAV Production Using HDAC Inhibitor

USPTO granted Patent US12612644B2 to REGENXBIO INC. on April 28, 2026, covering methods for producing recombinant Adeno-Associated Virus (rAAV) particles using histone deacetylase (HDAC) inhibitors. The patent names Michael Gillmeister, Miguel Valle, Robert Stadelman, Franz Gerner, Matthieu Guibert, and Bhargavi Kondragunta as inventors. The application (No. 17267247) was filed August 9, 2019, and the granted patent contains 14 claims.

Routine Notice Intellectual Property
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Harvard AAV Gene Therapy Patent for Hearing Loss, Blindness

The USPTO granted Patent US12612645B2 to President and Fellows of Harvard College on April 28, 2026. The patent covers isolated nucleic acids, vectors, and rAAV.9.PHP.B compositions encoding mini-PCDH15, along with methods for treating hearing loss and/or blindness, particularly Usher Syndrome type IF. The patent also covers gRNA associated with base editors to correct PCDH15 mutations. Biotechnology firms and researchers developing gene therapies for inherited hearing and vision disorders should review this patent landscape. The 15 granted claims provide Harvard with broad protection over AAV-mediated mini-PCDH15 expression for therapeutic applications.

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Live Imaging System to Visualize Retro-Transcribed Viral DNA Genome, Institut Pasteur, US Patent Grant US12613239B2

The USPTO granted US Patent 12,613,239 B2 to Institut Pasteur on April 28, 2026, covering a live imaging system for visualizing retro-transcribed viral DNA using the HIV-1 ANCHOR system. The patent claims a recombinant lentiviral vector with an ANCH sequence, a eukaryotic cell containing the integrated vector, and a method of observing lentiviral DNA through fluorescent protein detection. The invention was filed on April 11, 2020, under application number 17607118, with 18 claims. Applications include antiretroviral drug screening and potential extension to SARS-CoV-2 antiviral research.

Routine Notice Intellectual Property
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Aβ34 Antibody Diagnoses Alzheimer's, McGill Patent

USPTO granted patent US12613249B2 to The Royal Institution for the Advancement of Learning/McGill University covering an anti-Aβ34 antibody and its use for diagnosing Alzheimer's disease. The diagnostic method comprises obtaining a patient sample, detecting Aβ34 levels by contacting the sample with the anti-Aβ34 antibody, and diagnosing Alzheimer's when Aβ34 is detected alone or in combination with Aβ42 ratio analysis. The patent names inventors Gerhard Multhaup and Adeola Shobo and was granted on April 28, 2026.

Routine Rule Intellectual Property
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US12612638B2 - Fusion Constructs for Biopharmaceutical Polypeptide Expression in Cyanobacteria

The USPTO granted Patent US12612638B2 to The Regents of the University of California on April 28, 2026, covering fusion constructs designed to express biopharmaceutical polypeptides in cyanobacteria and microalgae. The patent names Anastasios Melis, Nico Betterle, Diego Hidalgo Martinez, and Andrew C. Saphire as inventors and includes 14 claims. The filing was received September 11, 2020, under application number 17642330. Patent holders and biotechnology firms developing cyanobacteria-based expression systems should review this grant for potential freedom-to-operate implications.

Routine Rule Intellectual Property
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US12613237B2 - Montana Molecular Biosensors for Detecting Arrestin Signaling

USPTO granted patent US12613237B2 to Montana Molecular, LLC on April 28, 2026, covering fluorescent reporter constructs and methods for detecting arrestin cellular signaling changes in cells. The patent, filed on July 30, 2019, includes 10 claims and CPC classifications in C07K, G01N domains. Inventors Thomas Hughes and Paul Tewson developed nucleic acid-based biosensors that can be packaged into vectors and cells for research and diagnostic applications targeting G-protein-coupled receptor signaling pathways.

Routine Rule Intellectual Property
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Phase 1b Study of TRICK-NK With T-Dxd in Treatment-Refractory Breast Cancers

A Phase 1b clinical trial (NCT07553390) evaluating TRICK-NK (TGFBR-2 KO CD70 CAR NK cells) in combination with trastuzumab deruxtecan (T-Dxd) in participants with treatment-refractory breast cancers has been registered. The study comprises dose escalation (Part 1), dose expansion (Part 2), and an optional schedule optimization phase testing shorter intervals between NK cell infusion and T-Dxd dosing. The trial will assess maximum tolerable dose and safety of the combination regimen.

Routine Notice Healthcare
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CMD Diet Pilot Trial for Recurrent Glioma Patients

This registry entry documents a new randomized, blinded interventional pilot study (NCT07553520) testing a cysteine/methionine deprivation (CMD) diet in up to 30 patients with recurrent glioma. Participants will be assigned to either a control diet or CMD diet for 2, 4, or 7 days before standard treatment, with researchers measuring glutathione metabolite levels, tumor cell behavior, and gut bacteria. Patients will be followed for progression-free survival and overall survival for up to 1 year.

Routine Notice Healthcare
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Phase 3 Trial Comparing Perioperative, Adjuvant, Neoadjuvant Toripalimab for Resectable Stage II-IIIA NSCLC

A randomized, open-label, multi-center Phase III clinical trial (NCT07554846) comparing three immunotherapy strategies—perioperative, neoadjuvant, and adjuvant—using Toripalimab in patients with resectable stage II-IIIA non-small cell lung cancer (NSCLC) without EGFR/ALK mutations. The trial, conducted by the Eastern Cooperative Thoracic Oncology Project (ECTOP) as protocol ECTOP-1030, is registered on ClinicalTrials.gov with an estimated start date.

Routine Notice Pharmaceuticals
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Hybrid Body Awareness Intervention for Menstrual Outcomes in Adolescent Girls

A new randomized controlled clinical trial registered as NCT07554053 will evaluate the effect of a hybrid body awareness-based intervention on menstrual symptoms, menstrual attitudes, and self-regulation levels in post-menarche adolescent girls. The study, registered April 28, 2026, lists 'Menstruation' and 'Adolescent Health' as conditions. Healthcare providers and clinical investigators researching adolescent menstrual health may need to be aware of this ongoing trial when considering similar interventions or study participation for their patients.

Routine Notice Healthcare
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Color Doppler Twinkling Artifact Imaging for Breast Clip Visibility in 86 Patients

A new single-center retrospective observational study (NCT07554781) was registered on ClinicalTrials.gov evaluating the color Doppler twinkling artifact feature to improve visibility of breast tissue marker clips within breast tissue and axillary lymph nodes. The study will enroll approximately 86 female patients with 110 clips who underwent breast tissue marker clip placement with corresponding preoperative imaging data from GE-10 or Siemens ultrasound systems between October 2024 and October 2025. The primary endpoint is the proportion of subjects whose implanted clips exhibit the characteristic twinkling artifact on color Doppler ultrasound imaging, reported with a 95% confidence interval.

Routine Notice Healthcare
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Photobiomodulation Laser for Reticular Pseudodrusen in AMD, 12-Month Trial

A randomized, sham-controlled Phase II clinical trial (NCT07554690) will evaluate whether photobiomodulation—a non-invasive low-energy laser therapy using specific wavelengths of light—can improve visual function and retinal structure in patients with early age-related macular degeneration who have reticular pseudodrusen. Participants (n=24) will be randomized to active photobiomodulation or sham treatment, with assessments over 12 months. The primary goal is to determine whether photobiomodulation can slow disease progression and improve low-light visual performance.

Routine Notice Healthcare
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A Multilevel Intervention to Prevent Noise Exposure in Farmworkers

This ClinicalTrials.gov registry entry describes a randomized controlled trial testing a multilevel hearing protection program for farmworkers exposed to occupational noise from machinery. Farms will be randomly assigned to receive the intervention (educational video, group discussion, and hands-on hearing protection training for workers; supervisor training) or to a comparison group. Participants will wear dosimeters during work shifts before the program and approximately one month later to measure noise exposure, and will complete surveys on knowledge, attitudes, and behaviors related to hearing protection. A subset of participants will be interviewed to assess barriers and facilitators to program implementation. Results are intended to inform future hearing health improvement efforts in agricultural settings.

Routine Notice Public Health
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Plasma Therapy for Diverse Wounds - 500-Patient Observational Study

A prospective, multicenter, real-world observational study (NCT07553689) evaluating plasma device therapy added to standard wound care has been registered with ClinicalTrials.gov. The study will enroll 500 patients receiving plasma therapy plus standard wound care and 500 matched controls receiving standard wound care alone across multiple hospitals in China. The primary outcomes include wound healing rate at 4 weeks, time to complete wound closure, pain relief, scar formation, and side effects, with follow-up extending up to 6 months. The study covers acute wounds (burns, surgical incisions), chronic wounds (diabetic foot ulcers, pressure injuries), post-grafting wounds, and sutured wounds.

Routine Notice Healthcare
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Feasibility Study of Co-designed Pre-radiotherapy Exercise Programme for Lung Cancer

A single-arm feasibility study will evaluate a co-designed, pre-radiotherapy exercise programme for patients with stage I-III non-small cell lung cancer. Participants will complete twenty, 20-minute supervised exercise sessions on a stationary exercise bike, performed immediately before each radiotherapy treatment at one of four personalised intensity levels. The study will monitor recruitment rates, session attendance, adherence to prescribed intensities, and adverse events to assess programme acceptability and safety, supplemented by qualitative interviews with participants, family members, and healthcare professionals.

Routine Notice Healthcare
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Bio-flexible Spinal Fixation Apparatus for Preventing Fatigue Fracture

USPTO granted Patent US12611232B2 to inventor Kyung-Woo Park on April 28, 2026, for a bio-flexible spinal fixation apparatus designed to prevent fatigue fracture after spinal fixation surgery. The device features an eccentric coil rod design allowing natural flexion and extension motion post-surgery, with the rod including a straight part and a coil part wound at a predetermined angle. The patent application (18329250) was filed June 5, 2023, and the patent contains 11 claims under CPC classifications A61B 17/7028 and A61B 17/7005.

Routine Rule Intellectual Property
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US12611233B2 Bone anchor housing limiter

The USPTO granted Patent No. US12611233B2 to Highridge Medical, LLC on April 28, 2026. The patent covers a bone anchor system comprising a fastener with a shaft, anchoring projection, and head; a rod housing connected to the fastener head; and a directional component with an outer diameter larger than the shaft diameter. The directional component includes a locking mechanism configured to engage the rod housing to limit housing movement during surgical fixation procedures. The patent contains 22 claims and was filed on January 23, 2024. Medical device manufacturers developing orthopedic surgical fixation products should evaluate this intellectual property for licensing or design-around considerations.

Routine Rule Intellectual Property
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Spinal Rod Patent US12611231B2, Spinal Resources, 28th Apr

USPTO granted patent US12611231B2 to Spinal Resources, Inc. on April 28, 2026. The patent covers spinal rods comprising at least two segments with different constant diameters connected by a tapered transition region, plus at least one curve extending along the segments. The filing date was December 7, 2023, with application number 18532262.

Routine Rule Intellectual Property
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Universal Fixator Clamp, Orthopedic Designs, Apr 28

USPTO granted patent US12611229B2 to Orthopedic Designs North America, Inc. on April 28, 2026, for a universal fixator clamp used in external fixation systems. The invention includes a torquing apparatus with multiple arms that engage complementary recesses in a proximal head to prevent patients from disengaging the clamp once tightened. The patent application (18612547) was filed on March 21, 2024, and the granted patent contains 6 claims.

Routine Rule Intellectual Property
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Spinal Fixation Polyaxial Pedicle Screw Assigned to VB Spine US Opco LLC

The USPTO granted US Patent 12611234B2 on April 28, 2026, to assignee VB Spine US Opco LLC for a polyaxial pedicle screw system used in spinal fixation surgeries. The patent, invented by Larry E. McClintock, contains 15 claims covering the screw's housing, bone screw member, friction plug, anvil, and compression ring or cap configuration. This grant establishes exclusive IP rights for the disclosed spinal fixation device architecture.

Routine Rule Intellectual Property
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Smith & Nephew Patent, Detachable Geared-Motor Strut Assembly for Spatial Frames

The USPTO granted Patent US12611228B2 to Smith & Nephew, Inc. on April 28, 2026, covering a detachable geared-motor assembly for motorizing a strut in a spatial frame. The patent claims priority to Application No. 18839091, filed February 14, 2023, and contains 23 claims under CPC classifications A61B 17/645, A61B 17/66, A61B 2017/00221, and A61B 2017/00398. Inventors include Paul Bell, Sied Janna, Darren J. Wilson, Andrew P. Noblett, Brian Roberts, Johnny R. Mason, and Scott Smyth. The geared-motor assembly is described as a standalone device including a microprocessor, printed-circuit board, and power supply for controlling the strut without external wires or a centralized controller. Competitors developing motorized spatial frame systems should review this patent for potential infringement exposure.

Routine Rule Intellectual Property
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Vanderbilt University Patent, Medical Device Delivery System

Vanderbilt University has received US Patent 12611227B2 titled 'Medical device delivery apparatus and method.' The patent covers a delivery device configured to deliver a medical device into a patient, including a distal ring, transition tunnel, and proximal chute. The patent was granted on April 28, 2026 with 18 claims and a filing date of May 28, 2021. This patent represents intellectual property protection for medical device delivery technology developed by Kent K. Higdon.

Routine Rule Intellectual Property
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Newmanbrain Brainwave Reading Apparatus Design USD1124354S1

The USPTO granted design patent USD1124354S1 to Newmanbrain, S.L. for a brainwave reading apparatus on April 28, 2026. The patent application was filed on October 22, 2024 under application number 29969433, with one claim covering the ornamental design of the device. The patent covers CPC classifications spanning brainwave monitoring, neurostimulation, and optical display components.

Routine Notice Intellectual Property
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Electrode Patch, USD1124357S1, Y-BRAIN INC

Design patent USD1124357S1 for an electrode patch for biological signal measurement was granted to Y-BRAIN INC. by the USPTO. The patent application was filed on April 30, 2025, assigned application number 30001972, with one design patent claim. The CPC classifications span multiple medical device categories including A61B 5/0404, A61B 5/0416, A61B 5/0422, A61B 5/0424, A61B 5/04012, A61B 5/04082, A61B 5/04085, A61B 5/04087, A61B 5/6841, A61N 1/046, A61N 1/0472, and A61N 1/0476.

Routine Notice Medical Devices
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Medtronic Implantable Cardiac Monitor Design Patent USD1124345S1

The USPTO granted Medtronic, Inc. Design Patent USD1124345S1 for an implantable cardiac monitor on April 28, 2026. The patent application was filed on April 30, 2024 under Application No. 29940020, with three inventors: Matthew T. Vanderpool, Michael R. Klardie, and Kris A. Peterson. The patent contains one design claim covering the ornamental appearance of the medical device.

Routine Rule Intellectual Property
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Electrode Patch Design Patent USD1124356S1 by Y-BRAIN INC

The USPTO granted Design Patent USD1124356S1 to Y-BRAIN INC on April 28, 2026, for an electrode patch for biological signal measurement. The patent was filed on April 30, 2025, under application number 30001969, with inventors Yoon Kyoung Hong, Tae Nam Kim, and Ki Won Lee. CPC classifications span A61B diagnostic/surgical categories and A61N electrotherapy categories.

Routine Notice Intellectual Property
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Nitrile SUMO Inhibitors for Cancer Treatment

The USPTO granted Patent US12612414B2 to CIT Therapeutics, Inc. on April 28, 2026, covering nitrile-containing compounds that inhibit Small Ubiquitin-like Modifier (SUMO) proteins. The patent includes 18 claims and names six inventors: Miles Douglas Kubota, Andrew S. Tasker, Fang-Tsao Hong, Mary Walton, Victor J. Cee, and Peter Buchowiecki. The compounds are directed toward use in cancer treatment, with CPC classification C07D 495/04 in organic chemistry.

Routine Notice Intellectual Property
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Vertex CFTR Modulator Patent Cystic Fibrosis Apr 28 2026

The USPTO granted Patent US12612416B2 to Vertex Pharmaceuticals Incorporated on April 28, 2026, covering modulators of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) with the core structure. The patent includes 23 claims and covers pharmaceutical compositions containing at least one such modulator, methods of treating cystic fibrosis, combination therapies, and processes and intermediates for making the modulators. The application was filed on October 6, 2021, under Application No. 18248065.

Routine Rule Intellectual Property
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Cystic Fibrosis Foundation Granted Patent on CFTR Potentiators

The USPTO granted Patent US12612409B2 to the Cystic Fibrosis Foundation on April 28, 2026, covering pyrrolopyrimidine compounds as potentiators of the Cystic Fibrosis Transmembrane conductance Regulator (CFTR). The patent names nine inventors and discloses pharmaceutical compositions and methods of treatment for cystic fibrosis, asthma, bronchiectasis, COPD, constipation, diabetes mellitus, dry eye disease, pancreatitis, rhinosinusitis, and Sjögren's Syndrome. The patent contains 20 claims and was filed under CPC classification C07D 487/04.

Routine Rule Intellectual Property
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BeOne Medicines I GmbH TLR7 Agonist Patent US12612407B2

The USPTO granted BeOne Medicines I GmbH patent US12612407B2 covering imidazo[2,1-f][1,2,4]triazin-4-amine derivatives and their stereoisomers and salts as TLR7 agonists for cancer treatment. The patent contains 14 claims and was applied for on February 6, 2020. This grant provides BeOne Medicines with enforceable intellectual property rights that may affect freedom-to-operate for other developers of TLR7-targeted cancer immunotherapies.

Routine Rule Intellectual Property
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Pyrazolone-Fused Pyrimidine Compound, Preparation Method and Applications Thereof

USPTO granted Patent US12612408B2 to Shanghai Pharmaceuticals Holding Co., Ltd. on April 28, 2026. The patent covers a pyrazolone-fused pyrimidine compound represented by formula (II) with improved inhibitory activity against WEE1 kinase, a protein target relevant to cancer therapy research. The filing date was June 28, 2020, under Application No. 17622579, with 20 claims allowed.

Routine Rule Intellectual Property
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Institut Pasteur Granted Patent on Imidazopyrazine Luciferin Derivatives

The USPTO granted Institut Pasteur patent US12612411B1 for imidazopyrazine derivatives, their preparation processes, and uses as luciferins in bioluminescence applications for biology and medicine. The patent, with 6 claims, covers CPC classifications C07D 487/04, A61K 49/0013, G01N 21/763, and G01N 33/573. Institut Pasteur now holds exclusive rights to these compounds, which have applications in bioluminescent assay and imaging technology development.

Routine Rule Intellectual Property
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Accro Bioscience Granted Patent, Heteroaryl Necrosis Inhibitors

USPTO granted patent US12612413B2 to Accro Bioscience (HK) Limited on April 28, 2026, covering heteroaryl compounds of Formula I as inhibitors of the programmed necrosis pathway, pharmaceutical compositions containing them, and methods of treatment using the same. The patent application (No. 17790728) was filed January 4, 2021, under CPC classification C07D 495/04, with 16 claims. Inventors are Xiaohu Zhang, Haikuo Ma, and Sudan He. This grant confers exclusive rights to the assignee for the patented subject matter, which relates to treating diseases and disorders arising from or related to programmed necrosis.

Routine Rule Intellectual Property
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Multi-cyclic IRAK and FLT3 Inhibiting Compounds and Uses Thereof

Children's Hospital Medical Center has been granted US Patent No. US12612410B2 for multi-cyclic compounds that inhibit IRAK and FLT3. The patent, filed on December 23, 2021 and granted on April 28, 2026, contains 20 claims covering pharmaceutical compositions and methods of treating diseases including hematopoietic cancers, myelodysplastic syndromes (MDS), and acute myeloid leukemia (AML). The invention also encompasses combination therapies with other cancer treatments.

Routine Rule Intellectual Property
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Nutshell Therapeutics Granted Patent for Nitrogen Sulfonamide Cancer Compounds

USPTO granted patent US12612402B2 to Nutshell Therapeutics (Shanghai) Co., Ltd. on April 28, 2026, covering nitrogen-containing fused heterocyclic compounds of N-sulfonamide and their use in cancer treatment. The patented compounds promote binding of p53 Y220C mutant with DNA and exhibit inhibitory activity against cancer cell proliferation. Three inventors are listed: Guoqiang Zhou, Liting Yu, and Caiming Xi. The patent application was filed on January 17, 2025, with 15 claims.

Routine Notice Intellectual Property
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Preparation method for (R)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid, derivatives thereof and levo-praziquantel

USPTO granted Patent US12612398B2 to Tongli Biomedical Co., Ltd. on April 28, 2026, covering a preparation method for (R)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid, derivatives thereof, and levo-praziquantel using immobilized lipase catalysis in a circulating fluidized bed reactor. The patent names five inventors: Jianping Wu, Lingjiao Tang, Xiao Zhan, Lirong Yang, and Mingxin Qian, with Application No. 17654974 filed March 15, 2022. The invention claims improved enzyme utilization, reduced enzyme/substrate ratio, mild reaction conditions, strong stereoselectivity, and high reaction efficiency. The patent contains 19 claims under CPC classification C07D 471/00.

Routine Notice Intellectual Property
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Opilan Pharma S1P Receptor Modulator Crystalline Forms Patent - US12612401B2

The USPTO granted Opilan Pharma Limited Patent US12612401B2 for crystalline forms of an S1P receptor modulator, a heterocyclic compound classified under CPC C07D 471/04. The patent covers the chemical compound (R)-5-(2,5-dichloro-4-(5-(8-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl)-1,2,4-oxadiazol-3-yl)phenoxy)piperidin-2-one, salts, and solvates. The patent issued on April 28, 2026, with 20 claims and inventors John Nuss, Jason Harris, Shendong Yuan, and Scott Alan Wolckenhauer.

Routine Rule Intellectual Property

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317 official sources tracked

ClinicalTrials.gov Studies

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USPTO Patent Grants - Diagnosis & Surgery (A61B)

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USPTO Patent Applications - Biotech (C12N)

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USPTO Patent Applications - Pharma (A61K)

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Regs.gov: Food and Drug Administration

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USPTO Patent Applications - Therapeutics (A61P)

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USPTO Patent Grants - Prosthetics (A61F)

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USPTO Patent Grants - Therapeutics (A61P)

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USPTO Patent Grants - Peptides (C07K)

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USPTO Patent Applications - Medical Devices (A61M)

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USPTO Patent Grants - Organic Chemistry (C07D)

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USPTO Patent Applications - Prosthetics (A61F)

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USPTO Patent Applications - Peptides (C07K)

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USPTO Patent Applications - Organic Chemistry (C07D)

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USPTO Trademarks - Medical Services (Class 044)

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USPTO Patent Applications - Health Informatics (G16H)

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USPTO Trademarks - Pharmaceuticals (Class 005)

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USPTO Patent Applications - Diagnosis & Surgery (A61B)

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USPTO Trademarks - Medical Devices (Class 010)

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EPO Patent Bulletin - Pharma (A61K)

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EPO Patent Bulletin - Diagnosis & Surgery (A61B)

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EPO Patent Bulletin - Medical Devices (A61M)

Updated 2d ago

EPO Patent Bulletin - Organic Chemistry (C07D)

Updated 2d ago

EPO Patent Bulletin - Biotech (C12N)

Updated 3d ago

USPTO Patent Grants - Medical Devices (A61M)

Updated 1h ago

EPO Patent Bulletin - Peptides (C07K)

Updated 3d ago

EPO Patent Bulletin - Health Informatics (G16H)

Updated 5d ago

Regs.gov: Centers for Medicare and Medicaid Services

Updated 23h ago

FR: Health and Human Services Department

Updated 5h ago

USPTO Patent Grants - Health Informatics (G16H)

Updated 3d ago

FR: National Institutes of Health

Updated 3d ago

EPO Patent Bulletin - Prosthetics (A61F)

Updated 2d ago

FR: Food and Drug Administration

Updated 3d ago

EPO Patent Bulletin - Therapeutics (A61P)

Updated 4d ago

USPTO Patent Grants - Pharma (A61K)

Updated 25m ago

FDA Warning Letters

Updated 1d ago

ISRCTN - UK Trials

Updated 16h ago

FR: Centers for Medicare & Medicaid Services

Updated 5h ago

WHO News

Updated 9h ago

MHRA Guidance & Safety

Updated 3h ago

South Carolina DPH News

Updated 3d ago

ClinicalTrials.gov - Phase 3 Trials by Start Date

Updated 8h ago

Regs.gov: Drug Enforcement Administration

Updated 3d ago

Brazil ANVISA

Updated 20h ago

IN Dept of Health

Updated 6d ago

ClinicalTrials.gov - Phase 4 Trials

Updated 8h ago

ISRCTN - Cancer Trials

Updated 24h ago

PAHO News

Updated 7h ago

FDA Drugs@FDA - New Applications and Actions

Updated 8h ago

Oregon OHA News

Updated 4d ago

USPTO Patent Grants - Biotech (C12N)

Updated 5d ago

FR: Centers for Disease Control and Prevention

Updated 7h ago

CMS Newsroom

Updated 5d ago

Hawaii DOH News

Updated 8h ago

NY DOH Press Releases 2026

Updated 6h ago

UK UKHSA

Updated 6h ago

UK DHSC

Updated 4d ago

Kansas KDHE Health News

Updated 3d ago

FR: Children and Families Administration

Updated 5h ago

ANZCTR - Clinical Trial Search

Updated 11h ago

Frequently asked

Where does the FDA publish drug approvals? +

The FDA publishes novel drug approvals on its Drugs Development and Approval Process pages, with the formal approval letter and labeling on Drugs@FDA. New drug applications, biologic license applications, and emergency use authorizations each have their own publication channel. GovPing tracks all of them, including the Federal Register entries that make the rules binding.

How do I track FDA medical device recalls? +

FDA medical device recalls publish on the FDA Recalls page, with a separate firehose for Class I (most serious), Class II, and Class III. Many recalls also generate Federal Register notices. For non-US devices, also watch MHRA in the UK, BfArM in Germany, and ANSM in France: products often hit those alerts days before US notification.

What is ClinicalTrials.gov and who has to register a trial? +

ClinicalTrials.gov is the NIH-run registry of clinical trials. By federal law, sponsors of Phase 2-4 studies of FDA-regulated drugs and devices must register the trial before enrolling patients and post results within a year of completion. The registry includes most international trials sponsored by US-based organizations. Non-compliance can trigger civil penalties under the FDA Amendments Act.

Where do hospital licensing actions get published? +

Hospital licensing actions live with state health departments, not the federal government. Each state DOH maintains its own discipline page. Joint Commission accreditation and CMS Conditions of Participation findings are tracked separately. GovPing covers state DOH actions for jurisdictions that publish them online and the federal CMS Survey & Certification surveys that drive Medicare reimbursement.

How fast does the FDA publish drug safety communications? +

Within 24 hours of a serious safety signal, in most cases. Drug Safety Communications and Drug Safety-related Labeling Changes publish weekly on the FDA's Drug Safety website, with REMS modifications and boxed warning additions handled separately. GovPing publishes each safety communication as it lands, with the affected drug, signal type, and recommended action parsed out.

How we track Healthcare & Life Sciences

  • GovPing monitors 317 official sources for this hub. Each source page is checked on a schedule, mostly every 15 minutes.
  • Every change includes a verbatim quote from the original page, a detection timestamp, and a stable URL back to the source.
  • No paid third-party feeds. No editorial filtering. Just what changed, who published it, and when.
  • Free to browse, free RSS, free email alerts.
Steve Butterworth

Curated by Steve Butterworth , founder of Changeflow. I track every government regulator that publishes a feed, classify changes by attention level, and write the editorial that frames them.

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