Wednesday, April 30, 2025 9:46:31 AM
You keep pushing the idea that RDGL missed its shot and is now limping around in a “generic business space.” But that’s either outdated thinking or willful spin, because the reality is very different in 2025.
1. This Isn’t a Commodity Market
Calling it “generic” ignores the most basic fact: there is no injectable Y90 gel on the market yet. Whoever gets there first defines the standard. RDGL’s one-pack, precision-targeted gel is leagues ahead of the old two-pack method you keep referencing—and that innovation is patent-protected. That’s how value is created in biotech.
2. Mayo and Telix Don’t Lend Their Names Lightly
You act like RDGL’s just paying Mayo to play along. That’s a lazy take. Mayo has reputational skin in the game and zero incentive to trial junk science. Same with Telix—why would a global oncology player waste time on something “generic”? Because they see what you don’t: a first-in-class injectable with real clinical upside.
3. The “Too Late” Argument Is Hollow
Biotech isn’t about who had the first idea—it’s about who gets execution and formulation right. RDGL didn’t rush half-baked data to market like others have. They took the hard road through FDA’s Class III device path. And now they’re weeks away from crossing the IDE line. That’s not failure. That’s precision.
4. India Strategy Is a Door-Opener, Not a Detour
Clinical data from India—especially through a partner like Karkinos—isn’t disqualified by geography. It’s judged by quality, and the FDA has accepted foreign data many times if it meets standards. RDGL manufacturing in India isn’t a weakness; it’s a smart global scale-up strategy.
5. MK’s Playbook Is Working
You keep throwing shade on MK, but look at the scoreboard: IDE submission finalized, FDA meeting done, Mayo locked in, Telix involved, Karkinos ready to launch trials. That’s what real leadership looks like. It’s not flashy—but it’s working.
RDGL’s not trying to compete in a generic commodity race. They’re building a precision oncology delivery platform. That’s a billion-dollar space. Whether they sell, scale, or partner, the upside absolutely still exists. And it looks like they’re finally executing.
$RDGL
1. This Isn’t a Commodity Market
Calling it “generic” ignores the most basic fact: there is no injectable Y90 gel on the market yet. Whoever gets there first defines the standard. RDGL’s one-pack, precision-targeted gel is leagues ahead of the old two-pack method you keep referencing—and that innovation is patent-protected. That’s how value is created in biotech.
2. Mayo and Telix Don’t Lend Their Names Lightly
You act like RDGL’s just paying Mayo to play along. That’s a lazy take. Mayo has reputational skin in the game and zero incentive to trial junk science. Same with Telix—why would a global oncology player waste time on something “generic”? Because they see what you don’t: a first-in-class injectable with real clinical upside.
3. The “Too Late” Argument Is Hollow
Biotech isn’t about who had the first idea—it’s about who gets execution and formulation right. RDGL didn’t rush half-baked data to market like others have. They took the hard road through FDA’s Class III device path. And now they’re weeks away from crossing the IDE line. That’s not failure. That’s precision.
4. India Strategy Is a Door-Opener, Not a Detour
Clinical data from India—especially through a partner like Karkinos—isn’t disqualified by geography. It’s judged by quality, and the FDA has accepted foreign data many times if it meets standards. RDGL manufacturing in India isn’t a weakness; it’s a smart global scale-up strategy.
5. MK’s Playbook Is Working
You keep throwing shade on MK, but look at the scoreboard: IDE submission finalized, FDA meeting done, Mayo locked in, Telix involved, Karkinos ready to launch trials. That’s what real leadership looks like. It’s not flashy—but it’s working.
RDGL’s not trying to compete in a generic commodity race. They’re building a precision oncology delivery platform. That’s a billion-dollar space. Whether they sell, scale, or partner, the upside absolutely still exists. And it looks like they’re finally executing.
$RDGL
Know what you own, and know why you own it.
Recent RDGL News
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 05/14/2026 08:45:22 PM
- Form 3 - Initial statement of beneficial ownership of securities • Edgar (US Regulatory) • 04/28/2026 08:44:48 PM
- Form QUALIF - Notice of Qualification [Regulation A] • Edgar (US Regulatory) • 03/06/2026 05:15:04 AM
- Form 1-A/A - Offering Statement [Regulation A]: [Amend] • Edgar (US Regulatory) • 03/04/2026 04:48:52 PM
- Vivos Inc. Diversifies Manufacturing Base with Planned U.S. and International Production Sites • GlobeNewswire Inc. • 02/17/2026 01:30:00 PM
- Vivos Inc. Announces Significant Progress Toward FDA Investigational Device Exemption (IDE) Submission for RadioGel® Precision Radionuclide Therapy™ • GlobeNewswire Inc. • 02/10/2026 01:30:00 PM
- Vivos Inc Updates Human Therapy Progress in India • GlobeNewswire Inc. • 02/03/2026 01:30:00 PM
- Vivos Inc. Strengthens Patent Protection with New U.S. Patent Issuance and PRECISIONGEL™ Trademark Approvals • GlobeNewswire Inc. • 01/28/2026 01:30:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 01/02/2026 04:06:21 PM
- Vivos Inc Summarizes Progress in its Animal Therapy Division • GlobeNewswire Inc. • 12/22/2025 05:56:08 PM
- Vivos Inc Summarzes Preogress in its Animal Therapy Division • GlobeNewswire Inc. • 12/22/2025 01:30:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 12/09/2025 09:00:31 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 11/21/2025 12:34:42 AM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/12/2025 11:08:03 AM
- Vivos Inc. Issues Shareholder Update Letter • GlobeNewswire Inc. • 11/06/2025 01:30:00 PM
- Vivos Inc. Strengthens Strategic Collaboration with Exubrion Therapeutics • GlobeNewswire Inc. • 10/29/2025 12:30:00 PM
- Vivos Inc. Retains Top FDA Regulatory Expert Dr. John J. Smith, M.D., J.D., to Support IDE Submission for RadioGel® • GlobeNewswire Inc. • 10/27/2025 12:30:00 PM
- Vivos Inc Board Authorizes Vivos Inc to Establish a Corporate Entity in India • GlobeNewswire Inc. • 09/29/2025 05:46:00 PM
- Vivos Inc Board Authorizes Vivios Inc to Establish a Corporate Entity in India • GlobeNewswire Inc. • 09/29/2025 12:30:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 09/18/2025 08:01:35 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 08/13/2025 07:32:46 PM
