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Lantern Pharma Reports First Quarter 2023 Financial Results and Operational Highlights Dosed first patient in the Phase 2 Harmonic clinical trial; a study for the unique population of non-small lung cancer patients who a

Key Takeaway: Lantern Pharma reported its first quarter 2023 financial results and announced key operational milestones. The company successfully dosed its first patient in the Phase 2 Harmonic clinical trial for non-small cell lung cancer targeting never-smokers. Additionally, Lantern anticipates submitting an IND application for LP-184 to the FDA and aims to launch Phase 1 trials for two new drug candidates in 2023. The company continues to leverage its AI platform RADR to streamline drug development and improve the speed and cost of bringing therapies to market.

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POSITIVE FACTORS

  • Successfully dosed the first patient in the Phase 2 Harmonic trial for non-small cell lung cancer.
  • Submission of IND application for LP-184 anticipated soon, targeting solid tumors.
  • AI platform RADR enhances drug discovery efficiency, potentially advancing new drug programs rapidly.

Full Press Release Details

Pharma Reports First Quarter 2023 Financial Results and Operational Highlights
Dosed first patient in the Phase 2 Harmonic clinical trial; a study for the unique population of non-small lung cancer patients who are never-smokers and who make up 15-20% of all lung cancer cases.
Submission of the IND application for LP-184 to the US Food and Drug Administration (FDA) is anticipated this week; a first-in-human Phase 1 clinical trial for LP-184, in genomically defined solid tumors, is targeted to launch in mid-2023.
Completion of IND-enabling studies for LP-284 is anticipated for mid-2023; a first-in-human Phase 1 clinical trial for LP-284, in multiple non-Hodgkin's lymphomas, is targeted to launch in the second half of 2023.
Received a notice of allowance from the United States Patent and Trademark Office (USPTO) for a composition of matter patent for LP-284.
Developed industry-leading AI algorithms to predict the blood-brain-barrier permeability of any compound; the algorithms have been fully incorporated into Lantern's AI platform RADR increasing its functionality.
Established an additional RADR collaboration with TTC Oncology to help advance their Phase 2 ready drug candidate TTC-352 in ER+ breast cancer.
$51.5 million in cash, cash equivalents, and marketable securities as of March 31, 2023.
Lantern has a cash runway into 2025.
Conference call scheduled for 4:30 p.m. ET / 1:30 p.m. PT today.
Wire)-Lantern Pharma Inc. (NASDAQ: LTRN), a clinical-stage biopharmaceutical company using its proprietary RADR
artificial intelligence ("AI") and machine learning ("ML") platform to transform the cost, pace, and timeline
of oncology drug discovery and development, today announced operational highlights and financial results for the first quarter ended
quarter we continued to execute our mission of transforming the oncology drug discovery and development process using our industry-leading
AI platform RADR . We are deploying AI at a massive scale - think millions of simultaneous instances of competing and
synergistic algorithms - to determine drug and cancer correlations that would be far too complex and time-consuming for any team of humans
to fully analyze, let alone replicate. AI is enabling us to understand and predict drug-cancer interactions, create new drug programs,
and discover cancer biology insights at a cost and timeline that was unimaginable in the near past, and Lantern Pharma is at the forefront
of this transformative approach," stated Panna Sharma Lantern's CEO and President.
part of our team's relentless efforts to advance RADR , we recently developed top-ranked and highly accurate algorithms
to predict any compound's blood-brain-barrier (BBB) permeability, which is one of the major obstacles to developing effective brain
cancer drugs. Continued innovations like this will position us for additional high-value biopharma collaborations and will also advance
our own AI-powered pipeline of brain and CNS cancer drug candidates," continued Sharma.
addition to our pioneering work transforming oncology drug discovery and development with AI, we continue to progress our drug candidates
into and through their clinical development. In March, we announced the dosing of the first patient in our Phase 2 Harmonic clinical
trial for never-smokers with NSCLC and anticipate enrollment will accelerate as we expand our sites across the US. Our team has been
unrelenting in their work to advance both LP-184 and LP-284 into first-in-human clinical trials this year. This week, we anticipate submitting
our IND application to the FDA for LP-184's first-in-human trial for advanced solid tumors and brain cancers. On average, we have
been able to advance our newly developed drug programs from initial AI insights to first-in-human clinical trials in 2-3 years and at
a cost of around $1.0-2.0 million USD per program - both metrics that are completely unheard of in oncology drug discovery," stated
of AI-Powered Pipeline:
of Starlight Therapeutics:
Platform Growth and Development:
Operational Highlights
Quarter 2023 Financial Overview:
Call and Webinar Details:
will host its first quarter 2023 earnings call and webinar today, Tuesday, May 9, 2023 at 4:30 p.m. ET.
https://us06web.zoom.us/webinar/register/2016825185534/WN_jlzd9TfkQMmU5eUH_gYfVw
Related presentation materials will be accessible at: https://ir.lanternpharma.com
A replay of the first quarter earnings call and webinar will be available at https://ir.lanternpharma.com .
Pharma is an AI company transforming the cost, pace, and timeline of oncology drug discovery and development. Our proprietary AI and
machine learning (ML) platform, RADR , leverages over 25 billion oncology-focused data points and a library of 200+ advanced
ML algorithms to help solve billion-dollar, real-world problems in oncology drug development. By harnessing the power of AI and with
input from world-class scientific advisors and collaborators, we have accelerated the development of our growing pipeline of therapies
including eleven cancer indications and an antibody-drug conjugate (ADC) program. On average, our newly developed drug programs have
been advanced from initial AI insights to first-in-human clinical trials in 2-3 years and at approximately $1.0-2.0 million per program.
Our lead development programs include two Phase 2 clinical programs and multiple upcoming Phase 1 clinical trials anticipated for 2023.
We have also established a wholly-owned subsidiary, Starlight Therapeutics Inc., to focus exclusively on the clinical execution of our
promising therapies for CNS and brain cancers, many of which have no effective treatment options. Our AI-driven pipeline of innovative
product candidates is estimated to have a combined annual market potential of over $15 billion USD and have the potential to provide
life-changing therapies to hundreds of thousands of cancer patients across the world.
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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 and ADC 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 and ADC candidates and to maximize their commercial potential by advancing such
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 December 31, 2022, filed with the Securities and Exchange
Commission on March 20, 2023. You may access our Annual Report on Form 10-K for the year ended December 31, 2022 under the investor SEC
filings tab of our website at www.lanternpharma.com or on the SEC's website at www.sec.gov. Given these risks and
uncertainties, we can give no assurances that our forward-looking statements will prove to be accurate, or that any other results or
events projected or contemplated by our forward-looking statements will in fact occur, and we caution investors not to place undue reliance
on these statements. All forward-looking statements in this press release represent our judgment as of the date hereof, and, except as
otherwise required by law, we disclaim any obligation to update any forward-looking statements to conform the statement to actual results
or changes in our expectations.
Pharma Disclosure Channels to Disseminate Information:
Pharma's investors and others should note that we announce material information to the public about our company and its technologies,
clinical developments, licensing matters and other matters through a variety of means, including Lantern Pharma's website, press
releases, SEC filings, digital newsletters, and social media, in order to achieve broad, non-exclusionary distribution of information
to the public. We encourage our investors and others to review the information we make public in the locations above as such information
could be deemed to be material information. Please note that this list may be updated from time to time.

Frequently Asked Questions

What is the Phase 2 Harmonic trial about?

The Phase 2 Harmonic trial targets non-small cell lung cancer patients who never smoked.

When will the IND application for LP-184 be submitted?

The IND application for LP-184 is anticipated to be submitted this week.

What is the status of LP-284's clinical trial?

Completion of IND-enabling studies for LP-284 is expected by mid-2023.

What is RADR's role in drug discovery?

RADR utilizes AI and ML to streamline oncology drug discovery and development.

How much cash does Lantern Pharma have?

Lantern had $51.5 million in cash, cash equivalents, and marketable securities as of March 31, 2023.

Last updated: May 9, 2023