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Friday, January 6, 2023

Immunome Stock Jumps On Discovery Pact With AbbVie

 

  • AbbVie Inc (NYSE: ABBV) and Immunome Inc (NASDAQ: IMNM) announced a worldwide collaboration and option agreement to discover up to 10 novel antibody-target pairs arising from three specified tumor types using Immunome's Discovery Engine.

  • Immunome will receive an upfront payment of $30 million. It will be eligible to receive additional platform access payments in the aggregate amount of up to $70 million based on AbbVie's election for Immunome to continue research using its Discovery Engine.

  • Immunome is also eligible to receive development and first commercial sale milestones of up to $120 million per target with respect to certain products derived from target-antibody pairs that AbbVie elects to purchase, with potential for further sales-based milestones as well as tiered royalties on global sales.

CureVac: Positive Data on Joint COVID-19 and Flu mRNA Vaccine Development Programs

 

  • Promising COVID-19 and flu modified mRNA vaccine candidates identified based on positive preliminary data from ongoing Phase 1 studies

  • All candidates use CureVac's advanced second-generation mRNA backbone optimized to achieve improved mRNA translation and strong immune responses at low doses

  • The preliminary results provide strong evidence of technology for CureVac's mRNA platform; CureVac and partner GSK plan to advance modified mRNA COVID-19 and flu candidates to the next stages of clinical development

  • COVID-19: monovalent modified mRNA vaccine candidate CV0501, encoding Omicron variant BA.1, successfully boosted antibody titers against BA.1 and the wild type variants and was generally well tolerated across all tested dose groups

  • Flu: monovalent modified mRNA vaccine candidate Flu-SV-mRNA successfully boosted antibody titers against matching flu strain; even at lowest dose, titers were at least in line with a licensed comparator; Flu-SV-mRNA was well tolerated across all tested dose groups

  • CureVac to host a webcast and conference call on January 6, 2023 at 3:00 p.m. CET / 9:00 a.m. EST. Access via the Investor Relations section of the CureVac homepage

CureVac will host a webcast and conference call on Friday, January 6, 2023 at 3:00 p.m. CET / 9:00 a.m. EST. The live conference call dial-in details and webcast link can be accessed via the Investor Relations section of the CureVac homepage at https://www.curevac.com/en/newsroom/events/

Corresponding presentation slides will be posted shortly before the start of the webcast. A replay will be made available at this website after the event.

https://finance.yahoo.com/news/curevac-announces-positive-data-joint-121500637.html

Madrigal: Additional Positive Results from Pivotal Phase 3 NASH Trial

 

  • As previously reported, resmetirom demonstrated improvements in NASH and liver fibrosis on liver biopsies, the primary endpoints of the MAESTRO-NASH trial

  • A supportive analysis using consensus reads of digitized biopsy images by the central pathologists replicated the positive primary endpoint results

  • These data will be presented at the NASH-TAG Conference on Friday January 6th, 2023

China in talks with Pfizer for generic COVID drug

 China is in talks with Pfizer Inc to secure a licence that will allow domestic drugmakers to manufacture and distribute a generic version of the U.S. firm's COVID-19 antiviral drug Paxlovid in China, three sources told Reuters.

China's medical products regulator - the National Medical Products Administration (NMPA) - has been leading the talks with Pfizer since late last month, one of the sources with knowledge of the matter said.

Beijing is keen to finalise licensing deal terms before the Lunar New Year which begins on Jan. 22, the source said.

Chinese hospitals are under intense pressure after the government abruptly abandoned its "zero-COVID" policy last month, sending infections soaring. The surging wave of infections across the country has overwhelmed hospitals, emptied pharmacies of medicines and caused international alarm.

Paxlovid, found to have reduced hospitalisations in high-risk patients by around 90% in a clinical trial, is in high demand with many Chinese attempting to get the drug abroad and have it shipped to China. Beijing has been largely resistant to western vaccines and treatments. Oral treatment Paxlovid is one of the few foreign ones it has approved.

In February last year, China approved Paxlovid, which was supposed to be largely available via hospitals, to treat high-risk patients in several provinces. Pfizer last month reached an agreement to export Paxlovid to China through a local company to make the medicine more widely available.

The NMPA and the State Council Information Office, which handles media queries for the government, did not respond to Reuters requests for comment.

A Pfizer spokesperson said the company is actively collaborating with Chinese authorities and all stakeholders to secure an adequate supply of Paxlovid in China.

All the sources declined to be identified as they are not authorised to speak to media.

The NMPA held a meeting with several Chinese drugmakers in late December to discuss preparations needed to make a generic version of Paxlovid hoping it would be able to secure the licence in the near future, two of the sources said.

Zhejiang Huahai Pharmaceutical, which signed a deal with Pfizer in August to produce Paxlovid only for use on the mainland, and CSPC Pharmaceutical Group, a developer of a potential mRNA COVID vaccine, are among those that attended the meeting, the first source said.

The second source said the NMPA has also advised firms to prepare to register with the regulator to produce the generic version of Paxlovid.

GENERIC DRUGMAKERS

Prospective candidates including Huahai and CSPC have in recent weeks been conducting "bioequivalence tests", which are required by Chinese regulators before generic drugs can be launched, the two sources and another source with direct knowledge of the matter said.

For a generic drug to be deemed equivalent to a branded medicine, such tests are required to make sure they work the same way in the body.

Both Huahai and CSPC expect to submit the tests results to the NMPA later this month, one of them added.

Huahai and CSPC did not respond to a request for comment.

In March, 35 generic drugmakers around the world including five Chinese firms agreed to make cheap versions of Paxlovid for 95 poorer countries through a licensing arrangement with the U.N.-backed Medicines Patent Pool (MPP). That licence does not allow the companies to sell generic Paxlovid in China.

The MPP licensing arrangement is royalty free for Pfizer, while COVID-19 remains classified as a "Public Health Emergency of International Concern" by the World Health Organization (WHO).

Following the pandemic period, sales to low-income countries will remain royalty free, lower-middle-income countries and upper-middle-income countries will be subject to a 5% royalty for sales to the public sector and a 10% royalty for sales to the private sector, MPP said at that time.

Due to severe shortages of antivirals as 1.4 billion Chinese battle infections, many have turned to underground channels to secure Paxlovid and other drugs, according to domestic media. Scalpers charge as much as 50,000 yuan ($7,260) for a box of Paxlovid, more than 20 times its original price of 2,300 yuan.

China has also pressed Pfizer to lower the price of Paxlovid as the government aims to include the drug in the national medical insurance scheme which could cover part of the cost, the three sources said.

https://www.yahoo.com/now/exclusive-china-talks-pfizer-generic-163742256.html

Nabriva Updates on Cash Preservation Plan

Company To Focus on Preserving Cash to Fund Orderly Wind Down of Operations-

-Company To Continue Work With Torreya Capital On Asset Monetization-

Nabriva Therapeutics plc (NASDAQ: NBRV) today announced that, after an assessment of strategic options, its Board of Directors approved a plan to preserve cash in order to adequately fund an orderly wind down of the Company’s operations.

As previously disclosed, the Company engaged Torreya Capital to facilitate the exploration of a range of strategic options, including potential in-licensing or out-licensing of commercial stage assets. While the Company continues to work with Torreya Capital on identifying and evaluating potential strategic options with the goal of maximizing shareholder value, the Company is currently focused on the sale of its existing assets, including Lefamulin and IV Fosfomycin.

https://finance.yahoo.com/news/nabriva-therapeutics-provides-corporate-120100923.html

Graphite Bio Shares Tank After Pausing Sickle Cell Therapy Study

 

  • Graphite Bio Inc (NASDAQ: GRPHvoluntarily paused the Phase 1/2 CEDAR study of nulabeglogene autogedtemcel (nula-cel) for sickle cell disease (SCD) following a serious adverse event in the first patient dosed with nula-cel.

  • The company concluded that the event is likely related to the study treatment.

  • As a result, the company will not meet its guidance for initial proof-of-concept data in mid-2023.

  • The decision by Graphite Bio to voluntarily pause the CEDAR study follows a serious and unexpected adverse event of prolonged low blood cell counts (pancytopenia) requiring ongoing transfusion and growth factor support in the first patient dosed with nula-cel.

  • The patient achieved study-defined neutrophil engraftment and has shown no evidence of myelodysplasia, a rare type of blood cancer.

  • Graphite Bio no longer expects to file an investigational new drug application for GPH102 in beta-thalassemia by mid-2024. The company is also working to identify operational efficiencies to extend its cash position to at least 2026.

  • Graphite Bio will provide a business update by the end of the first quarter of 2023.

Aligos on Track to Complete Phase 2-Enabling Activities in 2023 for NASH Candidate

 Final cohort of Phase 1 study projected to be complete in H1 2023 –

– Phase 2-enabling GLP toxicology studies projected to be complete in H2 2023 –

– Clinical update on all pipeline programs to be presented at the 2023 J.P. Morgan Healthcare Conference on January 12 at 10:30 a.m. PT –

https://finance.yahoo.com/news/aligos-therapeutics-track-complete-phase-130000041.html