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IOvA may be at $1 or lower before l its full approval. Only thing that matters here is IOVAs ability to cut costs drastically, increase revenue to exceed lowered target and NOT dilute shares at the lows. . This is asking a lot. Q2 will provide a nice glimpse. This stock has been played to the ground. Trust score is close to zero.
Cutting approval time by months can only be good for IOVA.
Let's see if the market agrees.
Potentially very good news for Iovance and for nsclc and endo approvals:
https://stocktwits.com/bavariaron/message/618601149
They analysts are a laughing stock. They are so behind the curve. If you bought based on their recommendation, you are screwed now. It’s at $2 for many good reasons. Repeated dilutions to ten time of $400M, lies about annual estimates, demand is low, burn rate is through the roof and additional dilutions are now a strong possibility. If they cannot ramp up sales and beat revised estimates hands down in Q2 and Q3, it’s game
over. $1 is more likely.
Based on 12 Wall Street analysts offering 12 month price targets for Iovance Biotherapeutics in the last 3 months. The average price target is $10.00 with a high forecast of $25.00 and a low forecast of $2.00. The average price target represents a 405.05% change from the last price of $1.98.
7 buy 5 hold 0 sell
https://www.tipranks.com/stocks/iova/forecast
A year ago, post approval for Amtagvi, share price shot up from $9 to $18. Today it is struggling at $2 mostly due to missed revenue, dilution of shares and loss of trust with current management team. CFO leaving at this juncture is proof positive of chaos. Only hope and prayer is the COO delivers on beating revised forecasts for the next several quarters while burn rate is controlled in a manner to reach breakeven by 2026. This coupled with good news from ongoing studies has the potential to bring the stock back to $9 (market cap $3B) by end of this year or early 2026. However, if they miss revised targets, it’s game over. This is my position and I’m sticking to it. Good luck to all of us. We need it to get out of this dire state.
From this point forward, what really matters is improving revenues each and every Q for the next several quarters. Despite what's happened in year one, the new CCO Mr. Kirby and his team have to be fully committed to improving the message of the need to have patients start TIL therapy far earlier in their disease progression. The KOL panel said that very same thing in the fireside chat the other day. There's plenty of catalysts for year two, but increasing revenues has to be at the top of the list by far.
Some have speculated that the CFO is leaving (or was asked to leave) due to the botched guidance (or the failure in messaging when it became obvious that guidance wasn't going to be met). It's important to remember that the CFO is only one piece in approving guidance before it goes out to the public. Likely the CEO and some BOD members were also part of that decision. If the CFO is being sacrificed, will there be others?
It's also possible that he's simply moving on as many execs do when they've been in a job for a certain number of years. If they wish to remain relevant, they make those customary job changes multiple times in their careers. Then again, he may simply be going to a job where they understand what he's saying, I always struggled with Jean-Marc's heavy accent on those conference calls.
In the meantime, IOVA is still a victim of the sector and the overall market until such time that they impress with increasing revenues. Q2 is looking like it'll suffice, but I suspect Q3 will finally show those improvements expected with the new CCO at the helm.
Many still want additional new leadership and I can't say that I blame them. Bottom line is the bottom line - revenues need to be increasing. Trusting this company's messaging again will take time.
GL to IOVA longs.
I am not sure it is a big loss given how they totally missed their FY25 guidance, it might help to restore some confidence between management and shareholders...
Happens all the time when other opportunities call.
"I was told I'd die from skin cancer - but my tumour disappeared with new therapy": https://inews.co.uk/news/health/skin-cancer-therapy-tumour-disappear-3726365
“The study demonstrates that for patients with few options left, a single infusion of lifileucel can provide a deep and lasting response and even complete remission in some cases. This marks a major advance in how we think about treating solid tumours.”
The next step is to help the onc docs to see TIL therapy as an earlier option, as a second line, not end of the line. This has shown to be even far more effective than these good results that we already see when used late in the disease progression.
Moving toward approval in foreign markets, numerous centers that did trials will become the first ATCs, centers that already have the experience necessary to hit the ground running.
GL
Jondoeuk, keeping with the goal of limiting off-topic, I chose to remove some posts that open the door to rebuttal. If I let one post stay up, I would need to allow responses which would then take us down that path again that we're trying to avoid.
Have a great day.
Spent a little time digesting the call and the transcript. Dr. Gastman was more conservative and obviously holding back a bit as is necessary when discussing trial data for lung. He can't definitively say without requiring an 8-K, but he most certainly implied that the numbers will be acceptable for the BLA which bodes well for us as shareholders.
Mr. Kirby was as expected, confident and focused. Exactly what I want from a CCO. Sales and marketing needed a lot more than they had previously and Kirby does seem like the real deal. It all depends on how effective they are at communicating with new docs, ATCs, and the entire medical teams necessary to start driving earlier referrals of patients. 3rd line+ is not going to cut it and they know that full well. Iovance needs more patients and earlier line patients to really impress and get that exponential growth that I believe is fully possible.
The big takeaway for me is the one we all know, lung is far bigger than the melanoma market, but melanoma is more than enough to be profitable. The slower start did reveal areas that needed attention but are fully correctible for the future success of Iovance. Melanoma was a great place to start and will make future indications pop much quicker upon their approvals now that many of those early bugs are worked out.
For me, the stock market just doesn't want to reward Iovance's past mistakes until some proof is given over the next couple Q's. Believability is still an issue.
End of the year should be bangin'.
GL to IOVA longs.
Bring back the institutional buyers!
https://www.tipranks.com/stocks/iova/forecast
Theorysuit, sorry, but I'm trying to keep off-topic pumping of other companies off this board so I requested removal of the full chain.
Here's hoping we can keep those types of posts to a minimum.
This will get all the bulls excited for years to come.
https://acrobat.adobe.com/id/urn:aaid:sc:VA6C2:8ed05d38-f968-4cc6-a2d7-5db87accc20a
Yeah the shorts keep doubling down. 28%. The only thing is that this company has a lot of connections to hedge funds on their board. WR, PD are both connected. We will see.
Well I jumped in nearly today and am already happy. Caught today's low. If nothing else I see the institutions buying and then shorting when it hits say $8- $10
Looks like another 9 million added to the short interest as of 5/30/25. It's now up to 86 million shares short.
The recent rally with money returning to biotechs will only be helped by the shorts needing to cover some of their positions.
Shorts become the buyers as I continue to add shares. I guess we're competing for those shares.
GL to IOVA longs.
Fireside chat at Goldman Sachs, June 11th, 1:20 pm ET: https://ir.iovance.com/news-releases/news-release-details/iovance-biotherapeutics-present-upcoming-conference
Thanks for the reply!
surfkast, there is no perfect reloading zone. You always seemed to struggle with Iovance and have been nothing but frustrated. This may be one of those companies that you just avoid. It's still going to be bumpy for the coming months and years. Management hasn't demonstrated that they have full control of this process yet, so risk is real and I don't know if your heart can take it.
I'm excited about the science. I'm still adding shares. I believe the company is worth more to most any BP that wants to expand into TIL therapy, but I'm not convinced that the current management team is the best choice for shareholders. It may be time to just get the best offer from BP so that the science can fully flourish even though it would only be a minor gain for most of us who are long shares. I'm fairly confident that the minimum value right now is still in the $4-5 billion range ($12-15/share). Many of my friends and I have average cost of shares below $10. Iovance is certainly worth a lot more once they demonstrate control over the manufacturing process with higher success rates and increasing profit margins. I do believe that they're starting to understand the need to be far more aggressive in their selling and marketing due to the complexities of this process and the challenges in the logistics.
I hate saying this because if they could go it alone, meaning they have a handle on how to grow this company properly and efficiently, IOVA could be a major winner with sales exceeding $2 billion in just a few years, and assuming lung approval down the road, $3-4 billion in sales in maybe less than 5 years. IOVA could get to $40-50/share or more with those kinds of numbers.
But my point remains, IOVA may be a bit too much for you to play anymore. It's not going to be an easy ride even if you're cost per share is around $2.
My attitude, if you're going to trade it, then trade it, but if you're going to invest for the long haul, buy now and walk away for 1 year.
Good luck to the longs.
Did I miss the perfect reloading zone? Do I still jump back in?
It's not that I wanted to sell but I had put some high and I didn't think it would get there and above all that it wouldn't come back! Oh well let's celebrate anyway! I still have some, but if it go down, I'll take back some more!
It's nice when insiders buy with their own money!
I agree with everything you have said. Very thoughtful. Hope you are right for our collective good. Let’s enjoy this beautiful sunny weekend! Cheers Badger🥂
Friday saw a 5+ million share block of IOVA stock trade in the after hours. Any thoughts?
Kirby, the CCO, did buy 30k shares himself in the open market the day prior: https://ir.iovance.com/static-files/20026620-7f04-474c-a36a-f87af3132207
https://ir.iovance.com/sec-filings/sec-filing/4/0001104659-25-057310
Feel free to read the Insider Trading Policy for Iovance (but it still won't guarantee that you'll understand why insiders buy or don't buy): https://www.sec.gov/Archives/edgar/data/1425205/000155837025001834/iova-20241231xex19d1.htm
Sunman, I still don't see the game the same way as you, but we're both taking this ride. I do agree that there were too many missteps and credibility is a hard thing to regain. I'm of the belief that the company is doing the right things now to correct for some of their past mistakes. For both our sakes, I hope I'm right and the company is learning and improving, and that your wrong regarding a plan to take this company private on the cheap.
We're riding together regardless so here's hoping for getting their act together and treating and ultimately helping and healing a great number of patients going forward.
The one thing we share in common is a belief in the science of TIL therapy being a very good option for a vast number of cancer patients.
I certainly hope we're not being played, and fwiw, I don't think we are. I think much of the guidance snafu was due to overzealous expectations that the initial ramp would go close to perfect. Failing to adjust for that overstatement sooner (or not even guiding) is still going to be a tough loss of confidence to overcome. Increasing revenues, margins, and successful new applications can cure a lot of our current concerns most certainly.
GL to us.
One year ago at this time it was at $18. Today, $2 makes you excited and you refer to it as a breakthrough!
The current interim CEO and his top line management team have lost credibility. Share price close to cash says it all. It remains under pressure and the ONLY way out of this mess is a blockbuster Q2 and Q3.
Firing of the CEO has a strong potential to add credibility.
A below par Q2 and Q3 means the end of IOVA for current common shareholders as the thugs would’ve succeeded in handing over the company for a liquidation fire sale for cheap.
Disclosure: I initiated a position at $1.75 and will sell half at $3. Will ride out the rest. Will add a bunch if it breaks $5 on solid lung cancer news and positive news from Amtagvi plus Keytruda trial as it would point to growing demand from the product while the company is learning to reduce COGS.
This is a brilliant response thank you! Yes you’re absolutely right it’s involved and time consuming.
jondoeuk, thanks for jumping in. There's just no helping this guy understand that this is an Iovance board. He posts his pretty pictures and graphs, he pumps his company of choice - a company on the verge of financial failure, he insults posters who don't fully agree with his interpretation of the science, and he simply has become a complete waste of time on this board. Some of his posts do get deleted for off-topic and for the equivalent of spam.
Any thoughts on how to educate someone who is so hell bent of causing confusion and spreading misinformation?
Thanks again for your info. Always appreciated.
Good luck to IOVA longs.
TIL therapy cannot stimulate Tscm cells vital for immune memory.
Which part of my posts is misinformation? Let IOVA retailers have their own judgements. They can tell if something is BS. By deleting my posts, you deprive them of the opportunity.
I almost hate posting this, but due to continual misinformation and lack of understanding from a certain poster who continually pumps a failing company on this board (Northwest Bio), I share the following AI generated response for clarity (I did not vet all of the info in this brief summary):
"T-cell stem cell memory (TSCM) cells and tumor-infiltrating lymphocytes (TILs) play a crucial role in cancer immunotherapy, particularly in adoptive T-cell therapy. TSCM cells, with their self-renewal and long-term persistence, are valuable for long-lasting anti-tumor immunity, while TILs, which are T cells that have infiltrated a tumor, are a source of tumor-reactive T cells for therapy.
.
TSCM cells are a type of memory T cell with stem-like properties, meaning they can self-renew and generate new T cells. They are characterized by their ability to persist for long periods and maintain their ability to respond to antigens. In cancer immunotherapy, TSCM cells are being explored as a potential source of T cells with superior long-term persistence and anti-tumor efficacy.
.
TIL therapy involves isolating T cells from the tumor microenvironment (TILs), expanding them in the lab, and then reinfusing them into the patient to target cancer cells. TILs are a valuable source of tumor-reactive T cells, as they have already been exposed to the tumor and have developed a specific anti-tumor response.
Relationship between TSCM and TILs:
.
TSCM cells can be present within the tumor and contribute to the pool of TILs. Furthermore, TILs can differentiate into memory T cell subsets, including TSCM, over time. Understanding the relationship between TSCM and TILs is important for designing effective adoptive T-cell therapies, as it may be possible to leverage TSCM cells to enhance the persistence and efficacy of TIL therapy.
Potential Benefits of TSCM in TIL Therapy:
.
By incorporating TSCM cells into TIL therapy, it is possible to enhance the long-term persistence and anti-tumor activity of the infused T cells. This could lead to a more durable anti-tumor response and potentially a higher rate of complete remission.
.
While TSCM and TILs hold promise for cancer immunotherapy, there are challenges to overcome. These include ensuring the T cells persist and do not become exhausted, as well as optimizing the conditions for expansion and reinfusion. Future research will focus on better understanding the factors that influence the differentiation and function of TSCM cells and TILs, as well as developing strategies to enhance their persistence and efficacy in adoptive T-cell therapies."
The future of cancer treatment will be the continual refinements of multiple approaches and optimizing any and all combinations that match best with specific cancer types. It's not one or the other, it's all at the same time and perfecting the match of meds and/or therapies at the best moment in the progression of the disease.
Pumping companies that are on the verge of financial failure like Northwest Bio, even if their science has hope, does not belong on the Iovance board. I don't know why this remains a difficult concept for certain individuals.
GL IOVA longs.
TIL therapy cannot stimulate Tscm cells vital for immune memory. It is not the incompetence of IOVA management that led the landslide of the sp. The true reason is the complete change of the landscape in cancer treatment. If Joseph Edelman is exiting, it doesn't bode well.
It is time consuming and labour intensive, consisting of whole-exome sequencing of DNA, RNA sequencing, creating tandem minigenes, requiring patient-specific monocyte-derived dendritic cells, and selecting the TIL to co-culture with the dendritic cells, before expansion of the neoantigen-reactive TIL. The time from resection to treatment was up to six months, often requiring bridging therapy.
There were a number of correlations with response, including fewer prior lines of therapy, number of neoantigen-reactive CD4+ TIL infused, and the number of neoantigens targeted by the TIL.
A much simpler and quicker method for Iovance would be enriching and expanding PD-1hiCD39+ and/or PD-1+ICOS+ CD4+ T-cells, and building off of that https://insight.jci.org/articles/view/142513 https://www.jci.org/articles/view/156821
Dstock is consistant at bringing little value to this board. Again, resectable vs unresectable, do you honestly not understand what you're posting?
This is all old news, it's always been part of the Iovance story, and regardless the success of these other approaches, Iovance will never have a shortage of patients to treat.
Spend a little more time understanding the science, the differences, the addressable market, and then go post all of that info somewhere else because your constant attempt to mislead on this board has grown tiresome.
You are a time bandit for anyone reading your posts.
GL to IOVA longs.
Another neoadjuvant checking point inhibitor treatment can reduce the number of lung cancer patients who otherwise come to IOVA for the 2nd line treatment.
Neoadjuvant Osimertinib for Resectable EGFR-Mutated Non-Small-Cell Lung Cancer
https://ascopubs.org/doi/pdf/10.1200/JCO-25-00883
Dstock, once again you're confused about the future of cancer treatment. It's a much bigger market that will continually be refined, where treatments will be far better matched to the specifics of each cancer, and where combination therapies will continue to become more commonplace, not less.
I'm glad to hear that you'll never be responding to me again - I feel free like I've never felt before.
This is just one type of neoadjuvant PD1 inhibitor treatment. More will come.
I didn't respond to you first. You replied to my post first.
Here I only talk about neoadjuvant PD1 inhibitor. Once DCVax-L has the approval, IOVA is going to have a hard time for its survival.
Exit this one while you can. This would be my last post to you.
How many patients could potentially benefit from TIL therapy? Does Iovance have the means to support all of them?
There is no shortage of patients for TIL therapy. Iovance has no concerns about all the patients that they won't see, they're focused on all of the patients that will need TIL therapy - which is far more than they will ever be able to handle (sadly).
You post like there's some magic pill out there that will some how eliminate the need for TIL therapy.
The person that doesn't get it is you. You continue to imply that Iovance is somehow going to suffer because some patients (thank goodness) will never need TIL therapy.
You state things that simply aren't true, your conclusions are ludicrous, and frankly, you're nothing more than an obsessive poster with little value offered to the discussion of Iovance and cancer treatment for that matter.
Try thinking before posting next time - and then don't post.
And you told me that you would never respond to me anymore - another post of yours that just wasn't true.
You simply cannot get it, can you?
Amtagvi is the 2nd line treatment, is it not? Neoadjuvant PD1 inhibitor treatment will significantly reduce the number of patients who have to seek the 2nd line treatment. Can you get it now?
Dstock once again doesn't understand what's he's posting. He actually hurts the knowledge base of investors with his incessant nonsense.
"Three cycles of neoadjuvant nivolumab plus chemotherapy significantly improved overall survival among patients with resectable NSCLC as compared with chemotherapy alone."
A resectable cancer by definition can be fully removed by surgery. If successfully removed, the likelihood of positive results following prophylactic treatment or any type of preconditioning with neoadjuvant treatment should be very high. Even without any other type of treatment, if you surgically remove the entire tumor and there's been no spread, the survival results will still be very good. The treatments are done to add a layer of protection just in case.
But here's the problem. What if the tumor is spreading, metastatic, unresectable? When you can show those results on unresectable cancers or metastatic cancers with additional metastases, you'll have something.
That's what TIL therapy can do that all these other treatments cannot do. Iovance is delivering on TIL therapy, and it will continue to be seen as a preferred choice for many types of solid tumor cancers where potential or known spread has occurred, or the tumor is not resectable due to location.
Amtagvi and all future TIL therapies will continue to be the preferred choice for metastatic or unresectable solid tumors. For the record, that's a huge market that we can only hope to catch a small percentage of currently.
GL to IOVA longs.
As a layman, I offer this with the understanding that my explanations may not be perfectly stated, but if anyone who is more skilled in the science wishes to add to this conversation, I'd greatly appreciate it.
Did I remind this board about the competition from neoadjuvant PD1 inhibitor in treating melanoma?
Now the new paper on treating lung cancer with neoadjuvant Opdivo in combination with chemo was published. Read it yourself. Amtagvi is going to have tough competition.
Overall Survival with Neoadjuvant Nivolumab plus Chemotherapy in Lung Cancer
https://www.nejm.org/doi/full/10.1056/NEJMoa2502931
"The Journal of Clinical Oncology Publishes Five-year Analysis of Amtagvi® (lifileucel) in Patients with Advanced Melanoma"
https://ir.iovance.com/news-releases/news-release-details/journal-clinical-oncology-publishes-five-year-analysis-amtagvir
Iovance Biotherapeutics is pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient.
Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer.
We are a patient-centric, collaborative organization that is driven to change the way cancer is treated. We are agile in our thinking and strive for excellence and innovation while acting with high integrity to create value for all stakeholders.
Tumor infiltrating lymphocytes (TIL) are naturally occurring immune cells that fight cancer. TIL are on constant surveillance to recognize, attack and kill cancer cells. When cancer invades and prevails, the TIL are unable to perform their intended function. Investigational TIL therapies are designed to reinvigorate a patient’s TIL to fight cancer. A patient’s naturally occurring TIL are collected and grown outside the body so they can be administered back to the patient as a one-time treatment. Once inside the body, Iovance TIL therapy deploys billions of personalized, patient-specific TIL to recognize and target diverse cancer cells.
TIL monotherapy and TIL combination therapies are being investigated in clinical studies in multiple advanced solid tumor cancers including melanoma, non-small cell lung cancer, cervical cancer and head and neck cancer.
AMTAGVI is the first FDA-approved T cell therapy for a solid tumor cancer and first treatment option for advanced melanoma after anti-PD-1 and targeted therapy
AMTAGVI deploys patient-specific immune cells that recognize and fight cancer
SAN CARLOS, Calif., Feb. 16, 2024 (GLOBE NEWSWIRE) -- Iovance Biotherapeutics, Inc. (NASDAQ: IOVA), a biotechnology company focused on innovating, developing and delivering novel polyclonal tumor infiltrating lymphocyte (TIL) cell therapies for patients with cancer, today announced that the U.S. Food and Drug Administration (FDA) has approved AMTAGVI™ (lifileucel) suspension for intravenous infusion. AMTAGVI is a tumor-derived autologous T cell immunotherapy indicated for the treatment of adult patients with unresectable or metastatic melanoma previously treated with a PD-1 blocking antibody, and if BRAF V600 mutation positive, a BRAF inhibitor with or without a MEK inhibitor. This indication is approved under an accelerated approval based on overall response rate (ORR) and duration of response. Iovance is also conducting TILVANCE-301, a Phase 3 trial to confirm clinical benefit.
AMTAGVI is the first and the only one-time, individualized T cell therapy to receive FDA approval for a solid tumor cancer. The proposed mechanism for AMTAGVI offers a new cell therapy approach that deploys patient-specific T cells called TIL cells. When cancer is detected, the immune system creates TIL cells to locate, attack, and destroy cancer. TIL cells recognize distinctive tumor markers on the cell surface of each person’s cancer. When cancer develops and prevails, the body’s natural TIL cells can no longer perform their intended function to fight cancer.
AMTAGVI is manufactured using a proprietary process to collect and expand a patient’s unique T cells from a portion of their tumor. AMTAGVI returns billions of the patient’s T cells back to the body to fight their cancer.* Authorized Treatment Centers (ATCs) will administer AMTAGVI to patients as part of a treatment regimen that includes lymphodepletion and a short course of high-dose PROLEUKIN® (aldesleukin).
https://ir.iovance.com/news-releases/news-release-details/iovances-amtagvitm-lifileucel-receives-us-fda-accelerated
File Date | Form | Investor | Prev Shares | Latest Shares | Δ Shares (Percent) | Ownership (Percent) | Δ Ownership (Percent) | |
---|---|---|---|---|---|---|---|---|
2024-03-01 | 13G | PERCEPTIVE ADVISORS LLC | 11,979,415 | 19,221,743 | 60.46 | 6.90 | 46.81 | |
2024-02-14 | 13G/A | Point72 Asset Management, L.P. | 8,114,890 | 468,821 | -94.22 | 0.20 | -96.00 | |
2024-02-13 | 13G/A | VANGUARD GROUP INC | 14,463,082 | 22,812,820 | 57.73 | 8.91 | -2.73 | |
2024-02-09 | 13G/A | MHR FUND MANAGEMENT LLC | 12,083,951 | 20,083,951 | 66.20 | 7.80 | 16.42 | |
2024-01-26 | 13G/A | BlackRock Inc. | 12,076,276 | 19,071,756 | 57.93 | 7.50 | -2.60 | |
2024-01-25 | 13G/A | STATE STREET CORP | 14,715,475 | 16,424,388 | 11.61 | 6.42 | -31.12 | |
2023-10-27 | 13D/A | Quogue Capital LLC | 20,000,000 | 25,000,000 | 25.00 | 15.84 | 26.52 | |
2023-02-14 | 13G/A | Avoro Capital Advisors LLC | 8,675,000 | 7,020,000 | -19.08 | 4.40 | -20.00 | |
2023-02-06 | 13G/A | WELLINGTON MANAGEMENT GROUP LLP | 9,584,082 | 421,610 | -95.60 | 0.27 | -95.58 |
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