Lantern Pharma to Present at Upcoming Scientific Conferences and Webinars
Lantern Pharma Inc. (NASDAQ: LTRN), a biopharmaceutical company utilizing its RADR® AI platform for oncology drug development, announced presentations at three upcoming events. CEO Panna Sharma will present on March 22 at the Rare Disease Innovation & Partnership Summit in Philadelphia, discussing AI in drug development. He will also participate in a free webinar on March 23, co-hosted by Science History Institute and American Chemical Society, focusing on AI's impact on drug discovery. Additionally, Peter Carr will moderate a session at the Genomics in Precision Oncology Xchange on April 5 in Boston, emphasizing clinical trial design.
For more information, visit www.lanternpharma.com.
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Rare Disease Innovation & Partnership Summit in
Philadelphia, PA onWednesday, March 22 at5:00 p.m. ET .Panna Sharma , CEO & President, will present.
Session Title: Using AI to Accelerate the Drug Discovery and Development Process for Rare Cancers
Registration Link: https://informaconnect.com/rare-disease-summit/pricing/
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How Artificial Intelligence Is Changing Drug Discovery Webinar on
Thursday, March 23 at1:00 p.m. ET .Panna Sharma , CEO & President, will be a panelist. The free webinar is co-hosted by theScience History Institute and theAmerican Chemical Society .
Webinar Link: https://www.eventbrite.com/e/how-artificial-intelligence-is-changing-drug-discovery
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Genomics in
Precision Oncology Xchange East Coast inBoston, MA onWednesday, April 5 at9:05 a.m. ET .Peter Carr , Principal Software Architect, will moderate a session for genomics informed clinical decisions.
Session Title: Clinical trial design & its use in silico modeling for combination therapies
Registration Link: https://www.hub-xchange.com/genomics-in-precision-oncology-east-coast-2023/
About
Please find more information at:
Website: www.lanternpharma.com
LinkedIn: https://www.linkedin.com/company/lanternpharma/
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Forward-looking Statements:
This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These forward-looking statements include, among other things, statements relating to: future events or our future financial performance; the potential advantages of our RADR® platform in identifying drug candidates and patient populations that are likely to respond to a drug candidate; our strategic plans to advance the development of our drug candidates and antibody drug conjugate (ADC) development program; estimates regarding the development timing for our drug candidates and ADC development program; expectations and estimates regarding clinical trial timing and patient enrollment; our research and development efforts of our internal drug discovery programs and the utilization of our RADR® platform to streamline the drug development process; our intention to leverage artificial intelligence, machine learning and genomic data to streamline and transform the pace, risk and cost of oncology drug discovery and development and to identify patient populations that would likely respond to a drug candidate; estimates regarding patient populations, potential markets and potential market sizes; sales estimates for our drug candidates and our plans to discover and develop drug candidates and to maximize their commercial potential by advancing such drug candidates ourselves or in collaboration with others. Any statements that are not statements of historical fact (including, without limitation, statements that use words such as "anticipate," "believe," "contemplate," "could," "estimate," "expect," "intend," "seek," "may," "might," "plan," "potential," "predict," "project," "target," "model," "objective," "aim," "upcoming," "should," "will," "would," or the negative of these words or other similar expressions) should be considered forward-looking statements. There are a number of important factors that could cause our actual results to differ materially from those indicated by the forward-looking statements, such as (i) the impact of the COVID-19 pandemic, (ii) the risk that our research and the research of our collaborators may not be successful, (iii) the risk that none of our product candidates has received FDA marketing approval, and we may not be able to successfully initiate, conduct, or conclude clinical testing for or obtain marketing approval for our product candidates, (iv) the risk that no drug product based on our proprietary RADR® AI platform has received FDA marketing approval or otherwise been incorporated into a commercial product, and (v) those other factors set forth in the Risk Factors section in our Annual Report on Form 10-K for the year ended
View source version on businesswire.com: https://www.businesswire.com/news/home/20230321005965/en/
Investor Relations Associate
ir@lanternpharma.com
Source:
FAQ
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