Latest Hotspot

New research shows Longhorn Vaccines and Diagnostics' Universal Flu Vaccine, LHNVD-105, triggers strong, durable immunity in lab animals

8 October 2023
3 min read

Longhorn Vaccines and Diagnostics LLC a "'One Health" enterprise involved in creating vaccines and diagnostic tools for global healthcare and zoonotic diseases, revealed fresh data highlighting the possible advantages of LHNVD-105, their universal influenza vaccine under development.

👇Please click on the image below to directly access the latest data (R&D Status | Core Patent | Clinical Trial | Approval status in Global countries) of this drug.

The research has displayed that LHNVD-105 prompts extensive and long-lasting immunity in mice against multiple human, bird, and pig influenza viruses. The information was released in one of the latest issues of the peer-reviewed Vaccines journal.

LHNVD-105 consists of complex peptides that are not linked, developed with a safe and potent adjuvant, the Army Liposome formula. The target of this is a variety of influenza antigens preserved from the hemagglutinin, neuraminidase, and matrix proteins.

The origin of influenza strains can be wild water birds and poultry, then pass on to pigs—serving as a channel for virus transmission—and then to humans, this could lead to another pandemic if outbreaks are not monitored. By merging multiple influenza strains into one multi-epitope peptide vaccination and formulating it with ALFQ, LHNVD-105 delivers an efficient super-seasonal vaccine that is cost-effective and readily scalable. This benefits public health by bringing it nearer to a practical approach for a global influenza vaccine and readiness for pandemics.

Longhorn Vaccines & Diagnostics CEO Gerald W. Fischer, MD, said, "The previously published research on LHNVD-105 indicated that an ALFQ-adjuvanted composite influenza peptide vaccine, which includes various highly preserved antigens of HA, NA, and matrix, triggered a strong and balanced immune response. 

The Vaccines study builds on these results by demonstrating the lockdown of the immune response and the range of influenza strains that the vaccine can shield, including human and avian viruses. The effectiveness of LHNVD-105 will continue to be tested as we seek a global solution to influenza prevention."

👇Please click on the picture link below for free registration or login directly if you have freemium accounts, you can browse the latest research progress on drugs, targets, organizations, clinical trials, clinical results, and drug patents related to this indication.

According to the data provided by the Synapse Database, As of October 5, 2023, there are 816 investigational drugs for the Influenza, including 87 targets, 555 R&D institutions involved, with related clinical trials reaching 3706,and as many as 61182 patents.

LHNVD-105, an artificial peptide vaccine, is under development by Longhorn Vaccines & Diagnostics LLC, aimed at combating human influenza. Despite being in its preliminary development stages, it shows potential as a prophylactic means against this contagious respiratory illness. Further exploration and clinical experiments are required to finalize its safety and effectiveness before it can become accessible for general use.

U.S. FDA Approves Takeda's ENTYVIO (vedolizumab) for continued treatment of severe active Ulcerative Colitis via under-the-skin injection
Latest Hotspot
3 min read
U.S. FDA Approves Takeda's ENTYVIO (vedolizumab) for continued treatment of severe active Ulcerative Colitis via under-the-skin injection
8 October 2023
Takeda announced U.S. FDA approval for ENTYVIO®(vedolizumab) subcutaneous delivery as a maintenance treatment for moderate to severe ulcerative colitis in adults, after initial intravenous therapy.
Read →
Initial Recipient of Omisirge™ (omidubicel-onlv) by Gamida Cell Administered to First Patient
Latest Hotspot
3 min read
Initial Recipient of Omisirge™ (omidubicel-onlv) by Gamida Cell Administered to First Patient
8 October 2023
Gamida Cell Ltd. has declared that the initial patient has been subjected to a stem cell transplantation procedure using Omisirge (omidubicel-onlv).
Read →
Abeona Therapeutics has requested a U.S. FDA Biologics License for expedited review of EB-101, a treatment for Recessive Dystrophic Epidermolysis Bullosa patients
Latest Hotspot
4 min read
Abeona Therapeutics has requested a U.S. FDA Biologics License for expedited review of EB-101, a treatment for Recessive Dystrophic Epidermolysis Bullosa patients
8 October 2023
Abeona Therapeutics Inc. has reported that they've lodged a BLA with U.S. FDA with a request to endorse EB-101.
Read →
AltruBio declares FDA approval on IND submission for ALTB-268, an Immune Checkpoint Booster, triggering a Phase 2 Clinical Study for dealing with Ulcerative Colitis
Latest Hotspot
3 min read
AltruBio declares FDA approval on IND submission for ALTB-268, an Immune Checkpoint Booster, triggering a Phase 2 Clinical Study for dealing with Ulcerative Colitis
8 October 2023
The US FDA approved AltruBio Inc.'s IND request, allowing Phase 2 clinical trials to start for its immune checkpoint booster, ALTB-268, for ulcerative colitis.
Read →
Get started for free today!
Accelerate Strategic R&D decision making with Synapse, PatSnap’s AI-powered Connected Innovation Intelligence Platform Built for Life Sciences Professionals.
Start your data trial now!
Synapse data is also accessible to external entities via APIs or data packages. Leverages most recent intelligence information, enabling fullest potential.