PaladinConqueror59
13 hours ago
You always insist that you're always always always right(nice try! nice try! rofl), but in fact you don't have any knowledge of patents, so you don't do anything but ask AI questions LOL!
Anyway, ENHANZE and HYBROZYME are completely different in patent material.
search the both patent and take a look at the details. Be sure to ask your patent attorney about the patent.
AZ SANDOZ Merck DAIICHI 'S patent attorneys are more smarter than you and AI.(in the field of patents)
In addition, MDASE claims extended rights as much as Earth's grains of sand, which is a big difference from the recent USTPO trend in the scope of rights.
Don't make any predictions, let's wait for the end of the dispute.
Hope/Misery
1 day ago
Interesting fact from 2017 which gives insight into why BMS operated Opdivo the way they did and let Keytruda take the lead.
Merck Announces Settlement and License Agreement Resolving KEYTRUDA® (pembrolizumab) Patent Litigation
Print
January 20, 2017 4:01 pm ET
Merck (NYSE:MRK), known as MSD outside the United States and Canada), and certain of its affiliates, today announced it agreed to enter into a settlement and license agreement with Bristol-Myers Squibb Company and Ono Pharmaceutical Co., Ltd., resolving the worldwide patent infringement litigation related to the use of an anti-PD-1 antibody for the treatment of cancer, such as KEYTRUDA® (pembrolizumab).
Under the settlement and license agreement, the company will make a one-time payment of $625 million to Bristol-Myers Squibb and provide royalties on the worldwide sales of KEYTRUDA for a non-exclusive license to market KEYTRUDA in any market in which it is approved. For global net sales of KEYTRUDA, the company will pay Bristol-Myers Squibb royalties as follows:
6.5 percent of net sales occurring from Jan. 1, 2017 through and
including Dec. 31, 2023; and
2.5 percent of net sales occurring Jan. 1, 2024 through and including
Dec. 31, 2026.
The parties also agreed to dismiss all claims in the relevant legal proceedings.
“Today’s announcement eliminates uncertainty and enables us to continue to focus on KEYTRUDA, our immuno-oncology medicine, which is already helping thousands of patients around the world and becoming a foundation for the treatment of cancer through our industry-leading clinical development program,” said Kenneth C. Frazier, chairman and chief executive officer, Merck.
The $625 million payment will be recorded in the company’s fourth-quarter and full-year 2016 results. This expense will be excluded from Merck’s non-GAAP results.
About Merck
For more than a century, Merck has been a global health care leader working to help the world be well. Merck is known as MSD outside the United States and Canada. Through our prescription medicines, vaccines, biologic therapies and animal health products, we work with customers and operate in more than 140 countries to deliver innovative health solutions. We also demonstrate our commitment to increasing access to health care through far-reaching policies, programs and partnerships. For more information, visit www.merck.com and connect with us on Twitter, Facebook, YouTube and LinkedIn.
Forward-Looking Statement of Merck & Co., Inc., Kenilworth, N.J., USA
This news release of Merck & Co., Inc., Kenilworth, N.J., USA (the “company”) includes “forward-looking statements” within the meaning of the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. These statements are based upon the current beliefs and expectations of the company’s management and are subject to significant risks and uncertainties. If underlying assumptions prove inaccurate or risks or uncertainties materialize, actual results may differ materially from those set forth in the forward-looking statements.
Risks and uncertainties include but are not limited to, general industry conditions and competition; general economic factors, including interest rate and currency exchange rate fluctuations; the impact of pharmaceutical industry regulation and health care legislation in the United States and internationally; global trends toward health care cost containment; technological advances, new products and patents attained by competitors; challenges inherent in new product development, including obtaining regulatory approval; the company’s ability to accurately predict future market conditions; manufacturing difficulties or delays; financial instability of international economies and sovereign risk; dependence on the effectiveness of the company’s patents and other protections for innovative products; and the exposure to litigation, including patent litigation, and/or regulatory actions.
The company undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise. Additional factors that could cause results to differ materially from those described in the forward-looking statements can be found in the company’s 2015 Annual Report on Form 10-K and the company’s other filings with the Securities and Exchange Commission (SEC) available at the SEC’s Internet site (www.sec.gov).
biotechinvestor1
3 days ago
You can cherry pick a particular time span and claim that halo has not done well. You picked 4 years. Well, how about 1 year (halo up 54% and both NASDAQ and S&P down)? Or how about 3 years (again halo outperformed both indexes)? How about 10 years (again halo outperformed indexes).
Those are too long for you? How about 6 months or year to date?
Too short for you? How about over its entire existence (halo outperformed handily)
You don't have to take my word for it. Do a chart of halo with comps against NASDAQ, S&P or XBI for yourselves.
Regardsing the Astra Zeneca, there may or may not have be an exclusivity barrier. Nonetheless, once MERCK loses the MDASE dispute , Astra Zenca will have to pay halozyme as well. Remember that MDASE patents dont expire until 2034. The only way they can avoid paying halozy is to not bring anything to market until 2034.
biotechinvestor1
4 days ago
Interesting how permabears are brushing off the important news from yesterday and are posting doom and gloom back and forth to each other in an echo chamber. The very conservative and skeptical JPM, Jessica Fye (whom perambears praise in their posts) adjusted her 2025 price target TO INCLUDE HALOZYME EARNINGS FROM KEYTRUDA SC. Keytruda is made by Merck. This means she believes Merck will sign a licensing agreement with halozyme in 2025.
Now, you permabears keep posting to each other as if nothing is going well. By the way, a Merck licensing agreement will be a significant deal as it will set the precedent for other deals to come (from all others who signed with alteogen)
My observation over the past 15 years on this board; nearly everytime the permabears increase the frequey of their nonsensical doom and gloom (eg "demand for enhanze has competely evaporated") postings, halozyme starts a major uptrend in shareprice. This one permabears was predicting doom when we were in low teens and single digits in 2018-2019. Look at the consistent and magnificent earnings growth and phat profit margins since then. Had you listened to him, you would have missed a 6x gain.
stockrafter
5 days ago
Well, back for a well deserved, "Tried to tell ya so.".......Looks like one FTR (For the Record) has proven correct........with little fanfare.....
It really isn't a SC injector per-say.....more of an Infusion SC injector.....note the "Tubing" which readers where directed to focus on in the other two HVAI injectors...............
PREFILLED AUTOINFUSION DEVICE
https://www.freepatentsonline.com/WO2025081072A1.html
Can't wait for other FTR to come to fruit.......such as hinted here..........nano nano.....
"34. The method of any one of claims 1-33, wherein the active ingredient is a small molecule, a peptide fragment, a biologic, or a nanoparticle. "
Whatever, let's hope Helen can sell it.........not batting to well on the others.......
Anyhoot..thanks for the comments........Way to go SR, .....Attaboy.......U R always welcome here with your dumb comments and hard facts......
stockrafter
1 week ago
Someone left the door open again, and guess who snuck in…….
BI1 stuff is okay good info but mostly just a summary of known info wishing for more info…..So this pesky investor quickly snuck in thru the open door again to leave some good speculative stuff…
First old news, but good news……depending on what one is interested in and how they connect the pieces…..…..
https://www.elektrofi.com/news/thermo-fisher-collaboration
New news…. Fisher recently stated……”In addition to traditional biologics, Thermo Fisher is expanding its mRNA capabilities through a collaboration with biotech company Elektrofi to establish a platform cGMP line to support Elektrofi’s planned clinical trials of self-injectable therapies. In late 2024, the companies successfully delivered the first lipid nanoparticle solution and in 2025 are progressing to drug product fill and clinical trial manufacturing. “
https://www.pharmamanufacturing.com/all-articles/article/55281157/thermo-fisher-grows-capacity-capabilities-for-its-pharma-services-in-strategic-expansion
And any investor with any interest would know by now, from you know who…….Elektorfi needs Enhanze for its self-injecting SC injections……but few are talking about it….
https://www.freepatentsonline.com/y2025/0082736.html
https://www.freepatentsonline.com/WO2025054552A1.html
191. The method of claim 124, wherein the composition is administered by a syringe or portable drug delivery injection device.
Or
224. A kit comprising: a syringe or portable drug delivery injection device; and a composition comprising: a plurality of particles suspended in a pharmaceutically acceptable liquid carrier, wherein substantially all of the particles comprise at least one therapeutic biologic or a salt thereof, and a hyaluronan degrading agent.
And knowing the personal connections between the two companies......if that info don’t scream a Halozyme combo deal in the making and soon to be announced.....….well blow me down……and kick me out……
With that said FTR………sneaking out of here again…….…..……