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Thursday, October 18, 2018 9:20:56 AM
https://seekingalpha.com/article/4212367-marker-therapeutics-safer-potentially-effective-car-t-alternative
Marker Therapeutics: A new start
I think that the only way to view the newly merged company is as a new company. Given the fervor for biotech IPO's this year, I was honestly a little surprised that Marker didn’t go it alone and do an IPO, but clearly they saw value in the combination of the two organizations. I have no doubt that part of that rationale is that both companies were similar in their goal which goes back to the beginning of this article regarding stimulating the immune system to safely eliminate cancer. CAR-T therapies do a fair job of eliminating cancer cells but safely? Not so much. I also believe that the leadership of the organization under Dr. Hoang, coupled with the outstanding scientific aptitude brought from Marker will be a fantastic combination. If you are considering this company, you SHOULD DEFINITELY spend an hour listening to Dr. Ann Leen's YouTube data presentation, and especially during the Q&A from 1:03-1:19. The rigor and rationale with which they've conducted Marker's studies so far is nothing short of impressive. The advisory board is no slouch either and includes multiple experts in cell therapies including recent Nobel Prize recipient Jim Allison.
When you look the Marker’s intelligent approach and data set of their technology in over 60 patients, and you overlay that with companies like Kite and Juno who won approved therapies with relatively small numbers of patients, and were then bought out for $11.9B and $9B respectively. The company should quickly become multiples of its current value.
Looking at other recent IPO examples, in particular Allogene (ALLO) which recently IPO'd with a value of over $3B, Marker would appear highly undervalued. Allogene is another CAR-T developer, but with a dataset that is aruguably less mature than Marker's and with a safety profile that is consistent with other CAR-T's. UCART19 had been previously on FDA hold due to patient deaths. In their summer 2018 data release with only 6 children in R/R B cell ALL, the data were interesting, but not fantastic. All patients experienced CRS, and other SAE's were observed. While 5 out of 6 experienced a CR, they all underwent allo-HST post-therapy and only 2 survived greater than 6 months post-HST. Allogenes product is differentiated from other CAR-T's, however, in that any donor's T cells can be used as opposed to a specific patient's. This is why many have referred to Allogene's therapy as an "off-the-shelf" CAR-T. It will still be far more expensive to produce than MultiTAA T cells.
Another recent notable IPO, was for Arvinas (ARVN). Arvinas currently has a $500M market cap for a cancer company that has not even entered clinical trials. Again, this is a pre-IND company with an interesting PROTAC cancer treatment paradigm. PROTAC therapies are designed to link proteins intended for destruction via the ubiquitination/proteasome system. Unlike Takeda's (OTCPK:TKPYY) Velcade, which inhibits the proteasome, PROTAC therapies are hoped to use the proteasome in order to "drug the undruggable" by selectively removing unwanted receptors or cell signaling mediators. While a fascinating therapy, they have never put medicine into a human and are not expected to treat their first patient until sometime in 2019.
I feel that if Marker had IPO'd, they probably could have commanded a market value closer to $2B. Fully diluted, that would give them a share price of around $29.41. I think that the time between the announcement of the merger and the late execution of the merger created a little apathy for TapImmune's share price. But with the successful completion of the merger in the rear view mirror, I believe that the merged company will appreciate in value quickly. I think that the rationale for the merger with TapImmune was built on their common interest in antigen-driven immune stimulation. Their approach was the only difference here, with TapImmune performing vaccinations with antigens intended to build an immune response and Marker doing the same ex vivo in culture. There may be crossover opportunities.
While it's difficult to rationalize a more traditional valuation for the company at this point, if a MultiTAA T cell product were to eventually hit the market at half of the price of the CAR-T therapies, the post Allo-HST AML market alone would probably represent over $1.8B annually. The lymphoma market in active disease could probably be 2x that, but I think the real value generator for Marker could be as maintenance therapy. Here, as an adjuvant maintenance therapy, in multiple cancer indications (including hematological malignancies and solid tumors) Marker could yield unprecedented revenues and would have no competition from CAR-T or any of the other traditional therapies, because all of them have adverse event profiles that would contraindicate their use for this. A cogent discussion around future run-rate revenue simply cannot be had at this point.
Recent MRKR News
- Form 8-K - Current report • Edgar (US Regulatory) • 06/12/2024 08:05:47 PM
- Form SC 13D/A - General statement of acquisition of beneficial ownership: [Amend] • Edgar (US Regulatory) • 05/17/2024 10:25:14 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 05/15/2024 08:40:16 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 05/15/2024 08:03:21 PM
- Principal Investigator from City of Hope National Medical Center Invited to Present Clinical Data from Marker Therapeutics APOLLO Study at 11th Global Summit on Hematologic Malignancies • GlobeNewswire Inc. • 04/08/2024 11:00:39 AM
- Marker Therapeutics Reports Year-End 2023 Corporate and Financial Results • GlobeNewswire Inc. • 03/25/2024 09:45:00 PM
- Marker Therapeutics to Present at the H.C. Wainwright 2nd Annual Cell Therapy Virtual Conference • GlobeNewswire Inc. • 03/22/2024 04:30:51 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/01/2024 01:02:47 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/26/2024 12:58:51 PM
- Marker Therapeutics Receives Approval from United States Adopted Name (USAN) Council and International Nonproprietary Names (INN) Expert Committee for “Neldaleucel” as Nonproprietary Name for MT-601 • GlobeNewswire Inc. • 01/22/2024 12:30:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/08/2024 01:30:48 PM
- Marker Therapeutics Announces Clinical Program Updates and Pipeline Prioritization • GlobeNewswire Inc. • 01/08/2024 01:24:49 PM
- Marker Therapeutics Announces Participation in Biotech Showcase and the 19th Annual Non-Dilutive Funding Summit During “J.P. Morgan Week 2024” • GlobeNewswire Inc. • 12/21/2023 04:00:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 12/11/2023 12:35:22 PM
- Marker Therapeutics Announces Sustained Complete Response in First Lymphoma Patient Treated with MT-601 following CAR T Relapse • GlobeNewswire Inc. • 12/11/2023 12:00:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/20/2023 09:37:41 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/09/2023 10:03:53 PM
- Marker Therapeutics Reports Third Quarter 2023 Financial Results and Provides Business Updates • GlobeNewswire Inc. • 11/09/2023 10:00:00 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/09/2023 09:31:53 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 09/11/2023 11:10:46 AM
- Marker Therapeutics Announces Complete Response in First Lymphoma Patient Treated with MT-601 after CAR T Relapse • GlobeNewswire Inc. • 09/11/2023 11:00:00 AM
- Marker Therapeutics to Present at the H.C. Wainwright 25th Annual Global Investment Conference • GlobeNewswire Inc. • 08/30/2023 12:00:38 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 08/14/2023 08:37:04 PM
- Marker Therapeutics Reports Second Quarter 2023 Financial Results and Provides Business Update • GlobeNewswire Inc. • 08/14/2023 08:30:27 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 08/14/2023 08:03:55 PM
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