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Wednesday, July 29, 2020 7:20:18 PM
On Sunday, Moderna (MRNA) disclosed it had been awarded an extra $472 million from the Biomedical Advanced Research and Development Authority (BARDA) to further support the development of mRNA-1273, its experimental COVID-19 vaccine. The new award follows a $483 million grant provided by BARDA in April, which means Moderna has now received a total of $955 million in funding from the U.S. government.
The award coincides with the initiation of Moderna’s Phase 3 study of mRNA-1273. The study began on Monday with the dosing of the first patients in the 30,000-participant study across 87 trial sites. If all goes according to plan, efficacy data for the study could become available as soon as Thanksgiving.
After gaining 298% since the turn of the year, Moderna shares experienced a rare setback last week following a ruling by the US Patent and Trademark Office (USPTO), which rejected Moderna’s claim that Arbutus Biopharma’s US patent on lipid nanoparticle (LNP) formulations should be revoked.
However, Chardan analyst Geulah Livshits argues the verdict will have little impact on Moderna’s COVID-19 vaccine program.
The 5-star analyst commented, “We would not anticipate IP negotiations to delay mRNA-1273 commercialization given the obviously important public health impact of a SARS-CoV-2 vaccine and the high degree of motivation among government agencies to roll out a vaccine as soon as possible. Moreover, we believe awards supporting development of mRNA-1273 and broader manufacturing scale-up reduce COGS across the platform and to us suggest Moderna's pipeline can become profitable even if royalty payments come into play in the future.”
To this end, Livshits rates MRNA a Buy along with a $95 price target, which implies nearly 20% upside from current levels. (To watch Livshits’ track record, click here)
When it comes to Moderna, Livshits’ colleagues hardly deviate from the Chardan playbook. MRNA's Strong Buy consensus rating is based on 13 Buy ratings and 4 Holds. The Street thinks a 17% premium will be added to MRNA shares over the next 12 months, going by the $90.67 average price target
The award coincides with the initiation of Moderna’s Phase 3 study of mRNA-1273. The study began on Monday with the dosing of the first patients in the 30,000-participant study across 87 trial sites. If all goes according to plan, efficacy data for the study could become available as soon as Thanksgiving.
After gaining 298% since the turn of the year, Moderna shares experienced a rare setback last week following a ruling by the US Patent and Trademark Office (USPTO), which rejected Moderna’s claim that Arbutus Biopharma’s US patent on lipid nanoparticle (LNP) formulations should be revoked.
However, Chardan analyst Geulah Livshits argues the verdict will have little impact on Moderna’s COVID-19 vaccine program.
The 5-star analyst commented, “We would not anticipate IP negotiations to delay mRNA-1273 commercialization given the obviously important public health impact of a SARS-CoV-2 vaccine and the high degree of motivation among government agencies to roll out a vaccine as soon as possible. Moreover, we believe awards supporting development of mRNA-1273 and broader manufacturing scale-up reduce COGS across the platform and to us suggest Moderna's pipeline can become profitable even if royalty payments come into play in the future.”
To this end, Livshits rates MRNA a Buy along with a $95 price target, which implies nearly 20% upside from current levels. (To watch Livshits’ track record, click here)
When it comes to Moderna, Livshits’ colleagues hardly deviate from the Chardan playbook. MRNA's Strong Buy consensus rating is based on 13 Buy ratings and 4 Holds. The Street thinks a 17% premium will be added to MRNA shares over the next 12 months, going by the $90.67 average price target
Recent MRNA News
- Moderna Announces Initiation of Phase 3 Study of Investigational mRNA Pandemic Influenza Vaccine Candidate • ACCESS Newswire • 04/21/2026 11:01:00 PM
- Moderna Announces Data to be Presented at 2026 ASCO Annual Meeting • ACCESS Newswire • 04/21/2026 02:00:00 PM
- Moderna Receives European Commission Marketing Authorization for mCOMBRIAX, Moderna's mRNA Combination Vaccine Against Influenza and COVID-19 • ACCESS Newswire • 04/21/2026 01:40:00 PM
- Moderna to Present at Upcoming Conferences in May 2026 • ACCESS Newswire • 04/21/2026 11:00:00 AM
- Moderna to Present Phase 1/2 Data on Its Investigational Cancer Antigen Therapy mRNA-4359 as First-Line Therapy in Combination with Pembrolizumab in Locally Advanced or Metastatic Melanoma at the 2026 AACR Annual Meeting • ACCESS Newswire • 04/17/2026 07:00:00 PM
- Moderna to Report First Quarter 2026 Financial Results on Friday, May 1, 2026 • ACCESS Newswire • 04/15/2026 11:00:00 AM
- Moderna to Present Revaccination Data for Its Investigational Seasonal Influenza Vaccine and for mRESVIA at ESCMID 2026 • ACCESS Newswire • 04/06/2026 10:01:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 04/06/2026 08:45:51 PM
- Form DEFA14A - Additional definitive proxy soliciting materials and Rule 14(a)(12) material • Edgar (US Regulatory) • 03/16/2026 08:32:27 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 03/16/2026 08:31:50 PM
- Form ARS - Annual Report to Security Holders • Edgar (US Regulatory) • 03/16/2026 08:31:08 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/06/2026 09:24:57 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/06/2026 09:21:25 PM
- Moderna agrees up to $2.25 billion settlement in COVID vaccine patent dispute • IH Market News • 03/04/2026 11:24:49 AM
- Moderna Resolves Global Patent Litigation with Arbutus/Genevant • ACCESS Newswire • 03/03/2026 09:15:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/03/2026 09:14:55 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/03/2026 09:10:53 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/03/2026 09:04:51 PM
- Form 144 - Report of proposed sale of securities • Edgar (US Regulatory) • 03/02/2026 02:56:47 PM
- European Medicines Agency's Committee for Medicinal Products for Human Use Adopts Positive Opinion Recommending Marketing Authorization of mCOMBRIAX, Moderna's mRNA Combination Vaccine Against Influenza and COVID-19 • ACCESS Newswire • 02/27/2026 12:00:00 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 02/25/2026 09:49:00 PM
- Form 144 - Report of proposed sale of securities • Edgar (US Regulatory) • 02/23/2026 03:26:22 PM
- Form S-8 - Securities to be offered to employees in employee benefit plans • Edgar (US Regulatory) • 02/20/2026 09:03:07 PM
- Form 10-K - Annual report [Section 13 and 15(d), not S-K Item 405] • Edgar (US Regulatory) • 02/20/2026 09:02:04 PM
- Moderna to Present at Upcoming Conferences in March 2026 • ACCESS Newswire • 02/19/2026 12:00:00 PM
