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glad i got back out before the drop.
Me too got a few also
grabbed some! quiet board, wow!
Shorts are on it big time
Shelf offering ahead
Unless another stock appears, BTAI will be No 1 on the Early Barchart Top 10
8.00 bucks in the making
Yaasss! An overreaction.
Bounce starting.
BioXcel Therapeutics' shares slumped Thursday after warning that prospects for regulatory approval for its investigational acute treatment for agitation in Alzheimer's patients could be hampered by a fraud investigation at a big study site.
In morning trading, the biopharmaceutical company's shares were 59% lower at $7.31 , having earlier in the day hit a fresh 52-week low of $7.09 . The stock is now down 66% so far this year..
BioXcel reported positive topline results from a late-stage trial that could support the use of BXCL501, an orally dissolving film formulation of dexmedetomidine, as a potential treatment for acute episodes of agitation in patients with mild to moderate Alzheimer's disease.
However, in a regulatory filing with the Securities and Exchange Commission , the company said it had confirmation that the principal investigator at a site that enrolled about 40% of the subjects in a Phase 3 clinical trial allegedly fabricated email correspondence. That came after BioXcel said it launched an investigation after learning in May the principal investigator in the so-called Tranquility II trial may have made up email correspondence purporting to demonstrate that the it timely submitted to the company's pharmacovigilance safety vendor a report of a serious adverse event from a different subject than one cited in a FDA form and purporting to show that the vendor had confirmed receipt.
The Food and Drug Administration inspected the clinical trial site in December, after which it issued a form identifying three observations related to the principal investigator's failure to adhere to an approved informed consent form for a limited number of subjects whose records the FDA reviewed, maintain adequate case histories for certain patients, and adhere to the investigational plan in certain instances.
BioXcel in its filing said it was made aware that fabricated email correspondence was provided to the FDA by the principal investigator's employer during the on-site inspection in December, and after unblinding the data it determined that the serious adverse event that was the subject of the correspondence between the principal investigator and pharmacovigilance vendor occurred in a subject in the placebo arm. It said the investigator hasn't participated in any other clinical trial sponsored or conducted by the company.
Meanwhile, BioXcel said topline results from the trial of BXCL501 were positive and the study met its primary efficacy endpoint. The 60 mcg dose also met the first key secondary endpoint of reducing agitation symptoms at one hour during the first episode of agitation, but didn't meet the other key secondary endpoint of change from baseline in PEC score at 30 minutes, the company said.
BioXcel Shares Drop Premarket Following Results for Phase 3 Trial of BXCL501
6:58 am ET June 29, 2023 (Dow Jones) Print
By Robb M. Stewart
BioXcel Therapeutics' shares were down sharply ahead of the bell after a late-stage trial of the biopharmaceutical company's investigation treatment for Alzheimer's disease-related agitation met its main target but missed one of the key secondary goals.
In premarket trading, the shares were 36% lower after ending Wednesday at $17.67, down 18% so far this year.
BioXcel said the topline results from its Phase 3 trial of BXCL501, an orally dissolving film formulation of dexmedetomidine, were positive and the study met its primary efficacy endpoint. The 60 mcg dose also met the first key secondary endpoint of reducing agitation symptoms at one hour during the first episode of agitation, but didn't meet the other key secondary endpoint of change from baseline in PEC score at 30 minutes, the company said.
Efficacy for the dose was supported by a number of secondary measures, and most patients responded to the first 60 mcg dose and were determined to be "very much" or "much improved" compared to 50% with placebo, BioXcel. It added the primary endpoint wasn't met for the 40 mcg dose.
Chief Executive Vimal Mehta said the results represent a milestone, and data from the Tranquility II trial show that BXCL501 has the potential to treat acute episodes of agitation in patients with mild to moderate Alzheimer's disease, if approved.
BioXcel said it plans to develop a path to potential supplemental new drug application submission for the acute treatment of agitation associated with Alzheimer's disease in the second half of the year, subject to further discussions with the Food and Drug Administration.
BXCL501 has been granted a breakthrough therapy designation for the acute treatment of dementia-related agitation based on Tranquility I data.
BioXcel Therapeutics to Ring Nasdaq Stock Market Closing Bell Today
NEW HAVEN, Conn., Feb. 21, 2023 (GLOBE NEWSWIRE) -- BioXcel Therapeutics, Inc. (Nasdaq: BTAI), a biopharmaceutical company utilizing artificial intelligence approaches to develop transformative medicines in neuroscience and immuno-oncology, today announced that Vimal Mehta, Ph.D., CEO of BioXcel Therapeutics, additional members of the management team, and other BioXcel team members will ring the closing bell of the Nasdaq Stock Market today, Tuesday, February 21, 2023.
"At BioXcel Therapeutics, we are building a disruptive biopharmaceutical business model to successfully drive accelerated AI-enabled drug development and commercialization," said Dr. Mehta. "Today we are celebrating a year of significant accomplishments that include FDA approval and launch of our first product, IGALMI(TM) sublingual film, for the acute treatment of agitation associated with schizophrenia or bipolar I or II disorder in adults. In addition, we look forward to market-expansion opportunities for our overall neuropsychiatric program, with two pivotal study readouts planned for BXCL501 in the first half of 2023. Recently, we also reported positive Phase 2 data for our lead immuno-oncology program, BXCL701, in combination with KEYTRUDA(R), which is in development for the treatment of a rare, aggressive form of prostate cancer. As BioXcel advances its lead drug candidates in two therapeutic areas, we appreciate Nasdaq's recognition of our progress through today's closing bell ceremony."
The ceremony will take place at the Nasdaq MarketSite, 4 Times Square, New York, beginning at 3:45 PM ET. It can be viewed at https://livestream.com/accounts/27896496/events/10752444.
Chugging down due to hawkish fed
BTAI is chugging right along.
First Patients Dosed in SERENITY III Phase 3 Trial for Acute Treatment of Agitation in Adults with Bipolar I or II Disorder or Schizophrenia
BioXcel Therapeutics Announces First Patients Dosed in SERENITY III Phase 3 Trial for Acute Treatment of Agitation in Adults with Bipolar I or II Disorder or Schizophrenia
SERENITY III will evaluate the efficacy and safety of BXCL501 for at-home use
Top-line pivotal data expected in 1H 2023
Estimated 23 million annual agitation episodes in the home-setting would more than double current market opportunity for BXCL501 in the U.S. (1) (-4)
NEW HAVEN, Conn., Nov. 30, 2022 (GLOBE NEWSWIRE) -- BioXcel Therapeutics, Inc. (Nasdaq: BTAI), a biopharmaceutical company utilizing artificial intelligence approaches to develop transformative medicines in neuroscience and immuno-oncology, today announced that the first 13 patients have been dosed in Part 1 of the pivotal Phase 3 SERENITY III trial investigating at-home use of BXCL501 (dexmedetomidine) sublingual film, the Company's proprietary, orally dissolving film, for agitation associated with bipolar I or II disorder or schizophrenia.
"Evaluating BXCL501 for at-home use is an exciting and important milestone that potentially expands the market opportunity for the treatment of agitation and drives the growth of our neuroscience franchise," said Robert Risinger, M.D., Chief Medical Officer, Neuroscience of BioXcel Therapeutics. "We anticipate top-line data from SERENITY III as well as our TRANQUILITY II trial for Alzheimer's-related agitation in the first half of 2023. These two near-term pivotal data readouts further reinforce the potential of BXCL501 to address the unmet medical needs of millions of patients."
The treatment of agitation represents a significant market opportunity. There are approximately 39 million reported agitation episodes that occur in the U.S. each year related to bipolar disorders and schizophrenia.(1) (-4) 23 million of these episodes occur outside of the institutional setting, potentially more than doubling the current market opportunity for BXCL501.
SERENITY III is a two-part, double-blinded, placebo-controlled pivotal study designed to evaluate BXCL501 60mcg dose for at-home use. This strategic trial design follows a Type B meeting with the U.S. Food and Drug Administration and observed dose-dependent responses in a prior Phase 1/2b study assessing a range of doses. The first part of the study is similar to SERENITY I and II and designed to assess the efficacy and safety of a 60mcg dose in acutely agitated patients with bipolar disorder or schizophrenia in a monitored setting. The primary efficacy endpoint is the change from baseline in Positive and Negative Syndrome Scale-Excitatory Component (PEC) total score at two hours after dosing compared to placebo. In Part 1, approximately 200 patients will be enrolled at up to approximately 20 clinical sites in the U.S. The second part of the study is designed to assess the safety of 60mcg dose compared to placebo when self-administered at home. SERENITY III will utilize many of the same investigators and clinical sites as SERENITY I and II.
BioXcel Therapeutics Q3 EPS $(1.49) Misses $(1.35) Estimate, Sales $137.00K Miss $1.09M Estimate
BofA lowers PT $BTAI $46 (was $52)Buy /Rev/EPS ests 22-24
BioXcel focused on the launch progress of Igalmi in the Co's 2Q22 update.
Co to focus on US growth4 Igalmi label expansion
The Co plans to expand Igalmi label in2 at-home setting along w other indications such as AD/MDD.
https://twitter.com/Quantumup1/status/1557113642692272130/photo/1
lowered revenue estimated from 17.4 to 3.5m for 2022
As of June 30, 2022, cash and cash equivalents totaled approximately $233.5 million. This excludes $30 million of contributions from the $260 million strategic financing announced in April. To date the Company has met the milestones and has received $100 million from the agreement.
BioXcel Therapeutics Reports Second Quarter 2022 Financial Results and Recent Operational Highlights
August 09 2022 - 07:00AM
BioXcel Therapeutics, Inc. (Nasdaq: BTAI), a commercial-stage biopharmaceutical company utilizing artificial intelligence approaches to develop transformative medicines in neuroscience and immuno-oncology, today announced its financial results for the second quarter ended June 30, 2022 and provided an update on key strategic initiatives.
“BioXcel Therapeutics made tremendous progress in its journey to becoming a fully integrated AI-driven commercial-stage company with the potential to transform the agitation treatment landscape,” said Vimal Mehta, Ph.D., CEO of BioXcel Therapeutics. “This transformation is being driven by the continued execution of our land and expand strategy within our neuroscience franchise. We are focused on the commercial launch for our recently FDA approved drug IGALMI™ while significantly increasing the opportunity for BXCL501 through at-home, medical setting expansion and the pursuit of multiple additional indications for our BXCL501 franchise. We believe we are well-positioned and have laid a strong foundation to drive long-term sustainable growth.”
Company Highlights
Neuroscience Franchise
IGALMI™ (dexmedetomidine) sublingual film
IGALMI was approved by the U.S. Food and Drug Administration (FDA) on April 5, 2022 for the acute treatment of agitation associated with schizophrenia or bipolar I or II disorder in adults.2 Within these two patient populations in the U.S., up to 25 million agitation episodes occur each year.3-5
Trade and Market Access: Key focus on unlocking access and supporting unencumbered demand generation for IGALMI.
IGALMI made available in 120mcg and 180mcg doses through the Company’s third-party logistics provider and for order through wholesalers as of early July.
Engagement underway with 59 high-value Integrated Delivery Networks (IDNs) and their affiliated hospitals.
Discussions and negotiations ongoing with major national Group Purchasing Organizations (GPOs), representing over 90% of beds in target hospitals.
Institutional Sales Force: Deployed first phase of our national sales force to target high-priority accounts in late May, with expansion of commercial footprint in process. Engaging multiple stakeholders in target hospitals and progressing P&T formulary review discussions. Gathered field level market intelligence which further reinforces and augments current and future commercial strategy.
Early response to the IGALMI value proposition exceeding expectations across full spectrum of institutional and healthcare stakeholders.
Market dynamics are rapidly evolving, favoring a less invasive and voluntary approach to treating agitation.
Marketing: Strategic marketing focused on branded campaigns to support sales force activities.
Peer-to-peer speaker programs educating healthcare providers (HCPs) of the importance of early intervention to mitigate agitation episodes.
Digital marketing efforts driving significant engagement resulting in over 100,000 visits to IGALMI HCP website.
Investigating Potential Expansion of BXCL501 for At-Home Use for Agitation Associated with Bipolar Disorders and Schizophrenia: Planning SERENITY III double-blinded, placebo-controlled, pivotal study designed to evaluate BXCL501 60mcg dose for at-home use. This strategic trial decision follows successful completion of Type B meeting with FDA and observed dose-dependent responses in a prior Phase 1/2b study assessing 60mcg, 80mcg, 120mcg, and 180mcg doses. Of the approximately 25 million agitation episodes that occur in the U.S. each year related to schizophrenia and bipolar disorders, approximately one-third occur outside of the institutional setting.6
SERENITY III will consist of two parts:
First part of SERENITY III is similar to the SERENITY I and II pivotal trials and designed to assess efficacy and safety in acutely agitated bipolar and schizophrenia patients.
Primary efficacy endpoint is change from baseline in Positive and Negative Syndrome Scale-Excitatory Component (PEC) total score at two hours after dosing compared to placebo.
Second part of SERENITY III designed to assess safety compared to placebo when self-administered at home.
SERENITY III will utilize many of the same investigators and clinical sites as SERENITY I and II and is expected to initiate in 2H 2022.
Clinical Pipeline
BXCL501, a proprietary, sublingual film formulation of dexmedetomidine, has received Breakthrough Therapy and Fast Track designation for the acute treatment of agitation associated with dementia.
Indication Expansion
Alzheimer’s Disease-related Agitation: TRANQUILITY program is designed to capture Alzheimer’s-related agitation market opportunity. There are an estimated 100 million agitation episodes in Alzheimer’s patients occurring in the U.S. annually.7
TRANQUILITY II: top-line data readout expected in 1H 2023.
TRANQUILITY III: enrollment expected to begin in 2H 2022.
Adjunctive Treatment for Major Depressive Disorder (MDD): Ongoing Phase 1 trial evaluating BXCL501 daily dosing designed to inform dose selection in future proof-of-concept study evaluating daily BXCL501 dosing in MDD patients. Over 300 million antidepressant prescriptions are filled annually in the U.S. and current treatments are limited by slow onsets of action and incomplete responses.8
Double-blind, placebo-controlled, multiple ascending dose (MAD) selection trial in healthy volunteers includes two cohorts of 18 patients, each having completed seven days of daily dosing of 30mcg or 60mcg compared to placebo.
Dose escalation in current cohort also enrolling to evaluate 80mcg.
Additional cohorts planned to evaluate safety and assess tolerability of a range of doses administered once daily and twice daily.
Top-line results expected in 1H 2023.
OnkosXcel Therapeutics
Established a wholly owned subsidiary to focus on the sustained expansion and optimization of the Company’s immuno-oncology (I-O) franchise, including its most advanced I-O program, BXCL701. BXCL701 is an investigational orally administered, systemic innate immune activator in development for the treatment of aggressive forms of prostate cancer.
Strategic Advancements: Fully functioning subsidiary dedicated to executing focused strategy and developing innovative oncology pipeline. Evaluating strategic options, which may include third party investments, aimed to fully capture unique value creation opportunity in areas of high unmet medical need.
Metastatic Castration-Resistant Prostate Cancer (mCRPC) Program: Continued ongoing Phase 2 trial for BXCL701 in combination with KEYTRUDA® (pembrolizumab) in mCRPC patients with small cell neuroendocrine carcinoma (SCNC) or adenocarcinoma phenotype.
Expect to complete enrollment of 28-patient SCNC cohort in 2H 2022.
Continued enrollment in adenocarcinoma randomized trial expansion evaluating BXCL701 monotherapy vs. BXCL701-KEYTRUDA combination therapy.
Corporate Updates
Strengthened Board of Directors: Appointed Michael P. Miller to the Company’s Board of Directors, to provide strategic leadership and commercial growth expertise.
Enhanced Intellectual Property: Received two Notices of Allowance for patents (issued from patent application numbers 17/560,392 and 17/560,423) related to IGALMI to cover film formulations containing dexmedetomidine and methods of treating agitation using the films.
Second Quarter 2022 Financial Results
Research and Development Expenses: Research and development expenses were $17.9 million for the second quarter of 2022, compared to $13.5 million for the same period in 2021. The increased expenses were primarily attributable to clinical trial costs related to the Company’s TRANQUILITY program.
Selling, General and Administrative Expenses: Selling, general and administrative expenses were $18.4 million for the second quarter of 2022, as compared to $14.1 million for the same period in 2021. The increase was primarily due to personnel and costs related to the launch of IGALMI in the U.S.
Net Loss: BioXcel Therapeutics reported a net loss of $37.7 million for the second quarter of 2022, compared to a net loss of $27.6 million for the same period in 2021.
As of June 30, 2022, cash and cash equivalents totaled approximately $233.5 million. This excludes $30 million of contributions from the $260 million strategic financing announced in April. To date the Company has met the milestones and has received $100 million from the agreement.
Conference Call
BioXcel Therapeutics will host a conference call and webcast August 9, 2022, at 8:30 a.m., ET, to discuss its second quarter 2022 financial results and provide an update on recent operational highlights. To access the call, please dial 877-407-5795 (domestic) and 201-689-8722 (international). A live webcast of the call will be available on the Investors section of the BioXcel website, www.bioxceltherapeutics.com, and a replay of the call will be available through November 9, 2022.
BioXcel Therapeutics may use its website as a distribution channel of material information about the Company. Financial and other important information regarding the Company is routinely posted on and accessible through the Investors sections of its website at www.bioxceltherapeutics.com. In addition, you may automatically receive email alerts and other information about the Company when you enroll your email address by visiting the “Email Alerts” option under the News/Events menu of the Investors & Media section of its website.
BioXcel Therapeutics Q2 EPS $(1.35) Misses $(1.22) Estimate
Mizuho Securities Initiates a Buy Rating on Bioxcel Therapeutics (BTAI)
August 04 2022 - 06:05AM
In a report released today, Graig Suvannavejh from Mizuho Securities initiated coverage with a Buy rating on Bioxcel Therapeutics (BTAI – Research Report) and a price target of $19.00. The company's shares closed last Wednesday at $14.91. According to TipRanks.com, Suvannavejh is a 2-star analyst with an average return of 0.7% and a 49.0% success rate. Suvannavejh covers the Healthcare sector, focusing on stocks such as Cerevel Therapeutics Holdings, Harmony Biosciences Holdings, and Intra-Cellular Therapies.
is BTAI in the XBI index?
Notice of Allowance received from USPTO
What is a Notice of Allowance?
A Notice of Allowance is a document sent to a patent applicant from the United States Patent and Trademark Office (USPTO) after a patent examiner has decided to issue the requested patent. The Notice of Allowance comes after the inventor has turned in a patent application and provided all information about the invention. This information includes the patent's description, design, drawings, or blueprints.
Since the Notice of Allowance shows the application is complete and meets all requirements, it is the final step in the long and complex patent application process. Your patent application has been fully reviewed and your invention has been given the green light for patenting. All that's left is to pay remaining fees and send any drawing corrections.
When a USPTO examiner feels an invention qualifies for a patent, he or she prepares a Notice of Allowance. When mailed to the inventor, the notice's mailing date is electronically recorded. If it will be published, the application requires both a publication and issue fee. Any fee requirements are listed in the Notice of Allowance. Applicants are also reminded to send an extra copy of the "Notice of Allowance and Fees Due" form when paying fees.
Once the issue fee has been paid, you'll be sent an Issue Notification letting you know your patent number and its anticipated issue date. Any extra patent applications based on the original "parent" application will need to be filed before the parent patent issue.
Eighteen months or more after the patent application's earliest filing date, the USPTO will publish the patent and it will be on public file.
https://www.investorvillage.com/uploads/87669/files/bioxcel-notice-USPTO.pdf
previous close 15.85 that had a gap to the open at 16.00 today.
took profits
Igalmi now available!
https://www.igalmihcp.com/
$BTAI Initiated @ Mizuho with a BUY $19 Target at the close
$BTAI Initiated @ Mizuho with a BUY $19 Target pic.twitter.com/eECwhCoSE8
— TheGodFatherKnows (@smantel) July 6, 2022
Patience pays off. Finally green in a treacherous market.
But the day is young.
On July 6, 2022, BioXcel Therapeutics, Inc. (the “Company”) announced that its product, IGALMI™ (dexmedetomidine), a sublingual film for the acute treatment of agitation associated with schizophrenia or bipolar I or II disorder in adults, is now available in doses of 120 and 180 mcg through the Company’s third party logistics provider and is available for order through wholesalers.
BioXcel Therapeutics Appoints Michael P. Miller to Board of Directors
July 05 2022 - 07:00AM
BioXcel Therapeutics, Inc. (Nasdaq: BTAI), a commercial-stage biopharmaceutical company utilizing artificial intelligence approaches to develop transformative medicines in neuroscience and immuno-oncology, today announced the appointment of Michael P. Miller to its Board of Directors, effective July 1, 2022. Mr. Miller brings nearly 40 years of strategic leadership and commercial growth experience in the pharmaceutical industry, where he most recently served as Executive Vice President, U.S. Commercial at Jazz Pharmaceuticals.
“We are pleased to welcome Mike to our Board and believe his deep commercial and market access expertise will be invaluable, especially now that the trade launch for IGALMI™ sublingual film is underway,” said Vimal Mehta, Ph.D., CEO of BioXcel Therapeutics. “Mike’s significant industry experience with initial and expanded-indication product launches, along with his development and operational knowledge in both neuroscience and oncology, will be a critical resource to the Company at this key time of growth, as we optimize our commercial capabilities and continue to advance our pipeline.”
While at Jazz Pharmaceuticals, Mr. Miller led a 450+ person commercial team that generated $2.3 billion in revenues in 2020. Prior to Jazz, he served in senior executive management positions with commercial, marketing, market access, and sales responsibilities at VIVUS, Genentech (until acquisition by Roche), Connetics Corporation, and ALZA Corporation. He began his pharmaceutical career at Syntex Laboratories in various commercial roles until its acquisition by Roche. Mr. Miller currently sits on the Board of Puma Biotechnology and serves as an advisor to several private and public biotechnology companies. He previously sat on the Board of the Leukemia and Lymphoma Society, Silicon Valley and Monterey Chapter. Mr. Miller holds a B.S. in Finance from the University of San Francisco and an M.B.A. from San Francisco State University.
“I am excited to join the Board of BioXcel Therapeutics at this pivotal time, as this is an innovative company that I believe has strong commercial potential and is well-positioned for growth driven by its AI-based drug discovery and development platform,” said Mr. Miller. “I look forward to bringing my expertise to support the ongoing IGALMI launch efforts and collaborating with the rest of the Board and management team to continue bringing transformative medicines to patients in need.”
Double bottom setup. $18.50 first target if it goes. 19M float with 20% short. GLTA $BTAI
blame H.C. Wainwright for Tuesday decline
They lowered the Buy from $134 to $110
At their conference Tuesday, management said expect revenue beginning in very early Q3. However Analyst expected revenue in Q2, although low.
EMA Paediatric Investigation Plan modification approved this week
That should grease skids for EMA marketing authorization application for Igalmi in adults.
https://www.investorvillage.com/uploads/87669/files/agenda-pdco-agenda-May-2022-meeting.pdf
BioXcel's Igalmi: Potential Market For Acute Agitation In Esquizofrenia And Bipolar Patients
https://seekingalpha.com/article/4512819-bioxcels-igalmi-potential-acute-agitation-esquizofrenia-bipolar
May 18, 2022 9:20 AM ETBioXcel Therapeutics, Inc. (BTAI)1 Comment3 Likes
Summary
BioXcel begins a new stage with IGALMI in the commercialization process.
With a current market cap of just $300 million, I think BioXcel offers an excellent investment opportunity right now.
I believe that BioXcel could reach a capitalization of between $1 billion and $1.5 billion without much trouble in the coming months.
BioXcel's Igalmi (dexmedetomidine oral film) was approved by the FDA on April 5 to treat acute agitation in patients with Schizophrenia and Bipolar syndrome. It is the first drug that BioXcel (NASDAQ:BTAI) manages to bring to market in its history. And most likely it will not be the only one, since the Company is currently conducting phase III trials with the same molecule (BXCL501) for another indication: Acute agitation in patients with Dementia and Alzheimer's, and the expectations are very good thanks to the very good results archived so far. As it is the first drug that BioXcel brings to the market, and there is no other similar drug to treat acute agitation in patients with Schizophrenia and Bipolar syndrome (there is only ADASUVE, but due to restrictive labeling, its sale potential is very limited), it is difficult to make a first estimate of the sales potential that IGALMI presents for this indication. In any case, we have some key data (number of annual attacks of agitation in this type of patient, the selling price of IGALMI, etc) thanks to which we can make a rough estimate of the revenue potential that IGALMI could have in the next years. What is interesting here is that, as I have already mentioned, the same drug is currently being tested for another indication (acute agitation in patients with Dementia and Alzheimer's), with exceptional results so far in terms of efficacy and safety profile, so if everything continues as planned (phase III top-line data are expected at the end of this year 2022), it would be expected to be approved for the first half of 2023. And the potential revenue for this last indication is between 4 and 6 times higher than the indication recently approved by the FDA.
What does this mean? Well, the initial sales of IGALMI in the coming quarters can give us an idea of the possible future revenue it will have once it is approved for the other indication (Dementia and Alzheimer's). In that sense, I think the first few quarters of sales growth will be slow, which is normal for any drug approved in its first few quarters, and within a few quarters is when I expect big sales growth.
BioXcel's share price has not stopped falling in recent weeks, practically at the same level as the entire Biotech sector. The inflation scenario and the latest rate hike by the Fed have made the markets nervous, reacting in a very exaggerated and bearish way. Many biotech companies are currently trading very undervalued. And it is precisely in this type of situation when you have to remain calm and take the opportunity to buy at really cheap prices knowing how to choose good companies with good fundamentals and a good cash position, because sooner or later purchases will return to the market, and these companies will be the ones that rise the most. BioXcel belongs to this group of companies.
The Company currently has a market capitalization of approximately $300 million. As we will see later, this capitalization implies a great undervaluation of BioXcel concerning IGALMI's revenue potential for the two indications that I have commented on previously. And all this without taking into account the other branch of its Pipeline: Oncology, with the candidate drug BXCL701, which is showing very promising efficacy in early phase trials to treat cancer resistant to first-line treatments. Therefore, I believe that BioXcel presents an unbeatable medium/long-term investment opportunity at current prices.
The potential market of IGALMI in Schizophrenia and bipolar Syndrome indication
BXCL501 will be marketed under the brand name IGALMI to treat acute agitation in patients with Schizophrenia and Bipolar syndrome. The initial date planned to start its commercialization is next May 24. The target will be patients who come to the hospital with agitation attacks. Subsequently, the Company plans to expand the use of IGALMI to other non-hospital settings. According to data provided by the Company, it is estimated that some 25 million attacks of agitation occur annually in patients of this type. Of all of them, about two-thirds are treated in hospitals. This gives us an initial patient target of around 16.5 million annually in the US.
What percentage of market penetration will IGALMI be able to take in the next 5 years?
This is a big question and difficult to answer. Currently, and as we have mentioned before, there is no drug specifically approved to treat this indication, except for ADASUVE, which, due to its restrictive labeling (many side effects), I practically do not consider to be a competitor for IGALMI. Until now, injectable or oral antipsychotics have been used to treat agitation in these patients, with many unpleasant side effects. There are also benzodiazepines (sedatives), which also have many side effects. Therefore, IGALMI is presented as a novel drug in this type of indication, highly effective and very safe, since it has practically no side effects. The FDA only recommends that its administration should be done under the supervision of a "health care provider", that is, any person in the health sector (doctors, nurses, caregivers, etc.), who can control blood pressure after administration. This is because a small percentage of patients in trials have experienced mild hypotension. The important thing here is that the FDA does not require the administration of IGALMI in a health facility, but rather that it can be administered even at home with the supervision of any health personnel, nurse, etc. This allows BioXcel to expand potential sales in the future. As it is the first drug to be commercialized by BioXcel, and as a small biotech company, without the commercial muscle of the big biopharmaceuticals, market penetration is expected to be slow and peak in the coming years. In my previous article, I estimated a maximum market penetration rate of 10%. I did this with a sale price of $150 per IGALMI film. We now know that BioXcel has lowered the selling price to $105 per film. Practically 33% lower than my first estimate. The Company argues in favor of this lower price that, after carrying out market studies, it is the best price to optimize sales. It is clear that the lower the price, the greater the demand. In fact, some analysts skeptical about IGALMI's commercial future argued that $150 was too expensive, since the alternative (antipsychotics and benzodiazepines can be found much cheaper). That's why I think the decision to lower the price is correct. In my estimation model of IGALMI's potential future revenues for this indication, I am going to increase the % of market penetration after the price reduction, up to 13%. I raise it by 30% (I calculated 10% initially) to compensate for the 33% reduction in the initial price of IGALMI.
So we have a peak annual potential revenue in the United States of:
16.6 millionX13%X$105=$226.59 million (This figure is based on very conservative numbers). Using a P/S ratio of 4 (before the interest rate increase I used to use a P/S ratio of 5, but I have now lowered it to 4 to reflect the greater future revenue discount due to higher rates), we get a value of $906.36 million.
This last figure would be an estimate only of the IGALMI value for the newly approved indication. As can be seen, a much higher value than BioXcel's current market capitalization (approximately $300 million). We will have to be attentive to the initial sales figures that will be reported from IGALMI during the second half of this year 2022. I expect slow (barring surprise) initial growth for later quarters this year 2022, and further sales growth for the next year 2023 once the commercial teams are up and running and Igalmi is better known.
For the other indication, Acute Agitation in Dementia and Alzheimer's patients, the expected revenue potential would be at least 4-5 times higher. This is because it is estimated that in the United States there are around 100 million attacks on this type of patient each year. And the figure continues to grow due to the high prevalence of Dementia and Alzheimer's in the most developed countries. Therefore, we would be talking about a peak potential annual revenue of approximately $1 billion. All this helps us to highlight the great potential for revaluation that BioXcel currently presents.
Risks
As with any biotech company, investors should consider some risks that could cause the share price to decline:
1- The Company intends to publish in the coming weeks the results of phase II of 40mg and 60mg to treat agitation in patients with Dementia and Alzheimer's. Although the expectations are very promising, there is always the risk that the results will not be as expected.
2- IGALMI's initial sales figures are lower than expected. This is the main risk I currently see. In any case, and as I have already mentioned, my very cautious estimate of maximum potential revenue is $226 million. And I have already commented that it would not be strange to see slow initial growth in sales, to then grow progressively at a higher rate once Igalmi will be best known.
3- Regarding a possible offering, I see it as very unlikely, after the agreement that the Company has recently signed with Qatar Investments under which BioXcel can use up to $260 million in the financing, which is added to the almost $200 million in cash that was reported in the last Q4 ER, allow the Company to finance its operations until at least 2024.
Conclusion
BioXcel begins a new stage with IGALMI in the commercialization process. My very conservative estimate of peak revenue for the indication of acute agitation in patients with Schizophrenia and Bipolar Syndrome is about 225 million dollars per year. For the other indication (Dementia and Alzheimer's) that figure should be 4 or 5 times higher due to the high prevalence of these diseases in more developed countries. For both indications, the annual peak revenue potential would be above $1.2 billion, which after applying a P/S ratio of 4x, would justify a long-term market capitalization of $4.8 billion. I believe that BioXcel could reach a capitalization of between $1 billion and $1.5 billion without much trouble in the coming months given the huge revenue potential of BXCL501 for both indications (acute agitation in patients with Schizophrenia+Bipolar disorder and Dementia+ Alzheimer's disease). With a current market cap of just $300 million, BioXcel offers an excellent investment opp
$BTAI CG Target $75. Predicts Alzh Dementia irritability success. Sees successful Institutional launch. Increases peak sales estimate ~50% ($934MM from $627MM) TAKEOVER CANDIDATE given approved neurology product scarcity.
$BTAI CG Target $75. Predicts Alzh Dementia irritability success. Sees successful Institutional launch. Increases peak sales estimate ~50% ($934MM from $627MM) TAKEOVER CANDIDATE given approved neurology product scarcity. pic.twitter.com/rh9h7kjT8Q
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