Phase 1/2 data demonstrates favorable tolerability; immunogenicity observed in 100% (44/44) of vaccinated subjects receiving 7.5 µg single dose & 5 µg single and prime-boost regimens
In primate challenge model, ARCT-021 demonstrates protection following both single dose and prime-boost regimens
In humoral immunodeficient animals depleted of B cells, ARCT-021 demonstrates protection with a single low dose administration, further emphasizing the potential importance of ARCT-021 cellular immunity
Phase 2 study to evaluate both single dose and prime-boost regimens in up to 600 participants
Anticipate interim Phase 2 data in early 2021; targeting global Phase 3 study start in Q2 2021
SAN DIEGO, CA, USA I December 28, 2020 I Arcturus Therapeutics Holdings Inc. (the “Company”, “Arcturus”, Nasdaq: ARCT), a leading clinical-stage messenger RNA medicines company focused on the development of infectious disease vaccines and significant opportunities within liver and respiratory rare diseases, today announced that the Company has received approval from the Singapore Health Sciences Authority to proceed with a Phase 2 clinical study of its vaccine candidate ARCT-021. This study will build upon the favorable Phase 1/2 study results, as well as supportive preclinical data.
“We are pleased to advance ARCT-021 into a Phase 2 study based upon our promising Phase 1/2 data, which continues to support the potential for Arcturus’ STARR™ self-replicating mRNA technology to provide a highly effective, and differentiated clinical profile, including a single dose regimen,” said Steve Hughes, M.D., Chief Development Officer of Arcturus. “The Phase 2 study will enable selection of the optimal ARCT-021 vaccination regimen for Phase 3 registrational studies. We look forward to obtaining interim Phase 2 data in early 2021 providing support for the anticipated initiation of a global Phase 3 study in Q2 2021.”
“The Phase 1/2 study results, together with recently generated preclinical data, indicate that ARCT-021 leads to a potent immune response to SARS-CoV-2, and demonstrates a differentiated biological profile whereby the immune response increases in the weeks following vaccination,” said Professor Ooi Eng Eong, Emerging Infectious Diseases Programme, Duke-NUS Medical School and a member of Arcturus’ Vaccine Platform Scientific Advisory Board. “The preclinical finding that ARCT-021 results in protection from SARS-CoV-2, even when humoral immunity is depleted, is particularly notable and suggests that ARCT-021 results in highly potent cellular immunity to the virus. Together, the body of data provides us with confidence that ARCT-021 vaccination will confer substantial protection from SARS-CoV-2 infection and COVID-19.”
Summary of Phase 1/2 Interim Clinical Data
Participant Description
- 106 participants; 78 received ARCT-021; 28 received placebo
- 44 participants received ARCT-021 at doses selected for Phase 2 – 27 young adults (≤ 55 years), and 17 older adults (> 55 years)
- 34 participants (22 young adults; 12 older adults) received a single administration of 5 µg
- 10 participants (5 young adults, 5 older adults) received a single administration of 7.5 µg
- 24 participants (12 young adults, 12 older adults) received a prime-boost regimen (5 µg x 2)
Safety and Tolerability
- No safety concerns identified
- No participants have withdrawn from the study; all participants completed all doses
- All adverse events except 2 were mild or moderate at doses selected for Phase 2
- Transient, asymptomatic Grade 3 lymphopenia seen in one participant. Lymphopenia has been observed with other RNA vaccines.
- Transient Grade 3 fatigue and myalgia observed following second injection in one older adult.
- Only serious adverse event (SAE) was in a placebo participant
Immunogenicity
- All (44/44) subjects receiving the 5µg or7.5 µg dose had humoral immune responses for binding (Luminex) and/or neutralizing antibodies (PRNT50)
- Binding antibody titers peaked through Day 43 for 5 µg and 7.5 µg single administration groups, and Day 57 for 5 µg prime-boost groups.
- Peak geometric mean binding antibody titers: 4,959 (5 µg single shot); 6,749 (7.5 µg single shot); 16,642 (5 µg prime-boost); placebo less than 400.
- Responder peak geometric mean neutralizing antibody titers of 32, 33 and 46, following 5 µg single dose, 7.5 µg single dose and 5 µg prime-boost participants, respectively.
- Neutralizing antibody titers in convalescent sera ranged from 12 to 1818.
- Cellular immune responses to SARS-COV-2 peptide pools evident by Day 15 for 5 µg and 7.5 µg doses
- PBMC ELISpot responses detected at Day 15.
- CD8+ and CD4+ T cell responses shown on cytokine staining (IFN-ϒ) at Day 29 following single dose at 5 µg and 7.5 µg and sustained at 2 weeks following boost at 5 µg.
- Th1 dominant CD4+ response following single dose and prime boost regimens.
New Preclinical Data Supports Protection from SARS-CoV-2
ARCT-021 vaccination effective in primate macaque challenge model
ARCT-021, both single administration and prime-boost regimens, are significantly effective in a primate challenge model. Vaccinated macaques show substantial reductions in lung viral titers. Preliminary data shows that lung viral titers are between 3.30 and 3.81 log lower in ARCT-021 vaccinated primates, in both single dose and prime-boost groups (see figure below), respectively. One week after SARS-CoV-2 virus challenge, geometric mean titers exceeded 1.31 x 104 in non-vaccinated primates compared with geometric mean titers of less than 10 in those vaccinated with ARCT-021.
ARCT-021 vaccination effective in humoral immunodeficient mice depleted of B cells
ARCT-021 vaccination (1 ug, single administration) is protective in animals depleted of B cells (see figure below). Notably, ARCT-021 vaccination was not effective in mice depleted of CD8+ T-cells suggesting that cellular immunity, specifically CD8+ T cells, plays a critical role in preventing SARS-CoV-2 infection.
About Arcturus Therapeutics
Founded in 2013 and based in San Diego, California, Arcturus Therapeutics Holdings Inc. (Nasdaq: ARCT) is a clinical-stage mRNA medicines and vaccines company with enabling technologies: (i) LUNAR® lipid-mediated delivery, (ii) STARR™ mRNA Technology and (iii) mRNA drug substance along with drug product manufacturing expertise. Arcturus’ diverse pipeline of RNA therapeutic and vaccine candidates includes self-replicating mRNA vaccine programs for SARS-CoV-2 (COVID-19) and Influenza, and other programs to potentially treat Ornithine Transcarbamylase (OTC) Deficiency, Cystic Fibrosis, and Cardiovascular Disease along with partnered programs including Glycogen Storage Disease Type 3, Hepatitis B Virus, and non-alcoholic steatohepatitis (NASH). Arcturus’ versatile RNA therapeutics platforms can be applied toward multiple types of nucleic acid medicines including messenger RNA, small interfering RNA, replicon RNA, antisense RNA, microRNA, DNA, and gene editing therapeutics. Arcturus’ technologies are covered by its extensive patent portfolio (200 patents and patent applications, issued in the U.S., Europe, Japan, China and other countries). Arcturus’ commitment to the development of novel RNA therapeutics has led to collaborations with Janssen Pharmaceuticals, Inc., part of the Janssen Pharmaceutical Companies of Johnson & Johnson, Ultragenyx Pharmaceutical, Inc., Takeda Pharmaceutical Company Limited, CureVac AG, Synthetic Genomics Inc., Duke-NUS Medical School, and the Cystic Fibrosis Foundation. For more information visit www.ArcturusRx.com. In addition, please connect with us on Twitter and LinkedIn.
SOURCE: Arcturus Therapeutics
Post Views: 73
Phase 1/2 data demonstrates favorable tolerability; immunogenicity observed in 100% (44/44) of vaccinated subjects receiving 7.5 µg single dose & 5 µg single and prime-boost regimens
In primate challenge model, ARCT-021 demonstrates protection following both single dose and prime-boost regimens
In humoral immunodeficient animals depleted of B cells, ARCT-021 demonstrates protection with a single low dose administration, further emphasizing the potential importance of ARCT-021 cellular immunity
Phase 2 study to evaluate both single dose and prime-boost regimens in up to 600 participants
Anticipate interim Phase 2 data in early 2021; targeting global Phase 3 study start in Q2 2021
SAN DIEGO, CA, USA I December 28, 2020 I Arcturus Therapeutics Holdings Inc. (the “Company”, “Arcturus”, Nasdaq: ARCT), a leading clinical-stage messenger RNA medicines company focused on the development of infectious disease vaccines and significant opportunities within liver and respiratory rare diseases, today announced that the Company has received approval from the Singapore Health Sciences Authority to proceed with a Phase 2 clinical study of its vaccine candidate ARCT-021. This study will build upon the favorable Phase 1/2 study results, as well as supportive preclinical data.
“We are pleased to advance ARCT-021 into a Phase 2 study based upon our promising Phase 1/2 data, which continues to support the potential for Arcturus’ STARR™ self-replicating mRNA technology to provide a highly effective, and differentiated clinical profile, including a single dose regimen,” said Steve Hughes, M.D., Chief Development Officer of Arcturus. “The Phase 2 study will enable selection of the optimal ARCT-021 vaccination regimen for Phase 3 registrational studies. We look forward to obtaining interim Phase 2 data in early 2021 providing support for the anticipated initiation of a global Phase 3 study in Q2 2021.”
“The Phase 1/2 study results, together with recently generated preclinical data, indicate that ARCT-021 leads to a potent immune response to SARS-CoV-2, and demonstrates a differentiated biological profile whereby the immune response increases in the weeks following vaccination,” said Professor Ooi Eng Eong, Emerging Infectious Diseases Programme, Duke-NUS Medical School and a member of Arcturus’ Vaccine Platform Scientific Advisory Board. “The preclinical finding that ARCT-021 results in protection from SARS-CoV-2, even when humoral immunity is depleted, is particularly notable and suggests that ARCT-021 results in highly potent cellular immunity to the virus. Together, the body of data provides us with confidence that ARCT-021 vaccination will confer substantial protection from SARS-CoV-2 infection and COVID-19.”
Summary of Phase 1/2 Interim Clinical Data
Participant Description
- 106 participants; 78 received ARCT-021; 28 received placebo
- 44 participants received ARCT-021 at doses selected for Phase 2 – 27 young adults (≤ 55 years), and 17 older adults (> 55 years)
- 34 participants (22 young adults; 12 older adults) received a single administration of 5 µg
- 10 participants (5 young adults, 5 older adults) received a single administration of 7.5 µg
- 24 participants (12 young adults, 12 older adults) received a prime-boost regimen (5 µg x 2)
Safety and Tolerability
- No safety concerns identified
- No participants have withdrawn from the study; all participants completed all doses
- All adverse events except 2 were mild or moderate at doses selected for Phase 2
- Transient, asymptomatic Grade 3 lymphopenia seen in one participant. Lymphopenia has been observed with other RNA vaccines.
- Transient Grade 3 fatigue and myalgia observed following second injection in one older adult.
- Only serious adverse event (SAE) was in a placebo participant
Immunogenicity
- All (44/44) subjects receiving the 5µg or7.5 µg dose had humoral immune responses for binding (Luminex) and/or neutralizing antibodies (PRNT50)
- Binding antibody titers peaked through Day 43 for 5 µg and 7.5 µg single administration groups, and Day 57 for 5 µg prime-boost groups.
- Peak geometric mean binding antibody titers: 4,959 (5 µg single shot); 6,749 (7.5 µg single shot); 16,642 (5 µg prime-boost); placebo less than 400.
- Responder peak geometric mean neutralizing antibody titers of 32, 33 and 46, following 5 µg single dose, 7.5 µg single dose and 5 µg prime-boost participants, respectively.
- Neutralizing antibody titers in convalescent sera ranged from 12 to 1818.
- Cellular immune responses to SARS-COV-2 peptide pools evident by Day 15 for 5 µg and 7.5 µg doses
- PBMC ELISpot responses detected at Day 15.
- CD8+ and CD4+ T cell responses shown on cytokine staining (IFN-ϒ) at Day 29 following single dose at 5 µg and 7.5 µg and sustained at 2 weeks following boost at 5 µg.
- Th1 dominant CD4+ response following single dose and prime boost regimens.
New Preclinical Data Supports Protection from SARS-CoV-2
ARCT-021 vaccination effective in primate macaque challenge model
ARCT-021, both single administration and prime-boost regimens, are significantly effective in a primate challenge model. Vaccinated macaques show substantial reductions in lung viral titers. Preliminary data shows that lung viral titers are between 3.30 and 3.81 log lower in ARCT-021 vaccinated primates, in both single dose and prime-boost groups (see figure below), respectively. One week after SARS-CoV-2 virus challenge, geometric mean titers exceeded 1.31 x 104 in non-vaccinated primates compared with geometric mean titers of less than 10 in those vaccinated with ARCT-021.
ARCT-021 vaccination effective in humoral immunodeficient mice depleted of B cells
ARCT-021 vaccination (1 ug, single administration) is protective in animals depleted of B cells (see figure below). Notably, ARCT-021 vaccination was not effective in mice depleted of CD8+ T-cells suggesting that cellular immunity, specifically CD8+ T cells, plays a critical role in preventing SARS-CoV-2 infection.
About Arcturus Therapeutics
Founded in 2013 and based in San Diego, California, Arcturus Therapeutics Holdings Inc. (Nasdaq: ARCT) is a clinical-stage mRNA medicines and vaccines company with enabling technologies: (i) LUNAR® lipid-mediated delivery, (ii) STARR™ mRNA Technology and (iii) mRNA drug substance along with drug product manufacturing expertise. Arcturus’ diverse pipeline of RNA therapeutic and vaccine candidates includes self-replicating mRNA vaccine programs for SARS-CoV-2 (COVID-19) and Influenza, and other programs to potentially treat Ornithine Transcarbamylase (OTC) Deficiency, Cystic Fibrosis, and Cardiovascular Disease along with partnered programs including Glycogen Storage Disease Type 3, Hepatitis B Virus, and non-alcoholic steatohepatitis (NASH). Arcturus’ versatile RNA therapeutics platforms can be applied toward multiple types of nucleic acid medicines including messenger RNA, small interfering RNA, replicon RNA, antisense RNA, microRNA, DNA, and gene editing therapeutics. Arcturus’ technologies are covered by its extensive patent portfolio (200 patents and patent applications, issued in the U.S., Europe, Japan, China and other countries). Arcturus’ commitment to the development of novel RNA therapeutics has led to collaborations with Janssen Pharmaceuticals, Inc., part of the Janssen Pharmaceutical Companies of Johnson & Johnson, Ultragenyx Pharmaceutical, Inc., Takeda Pharmaceutical Company Limited, CureVac AG, Synthetic Genomics Inc., Duke-NUS Medical School, and the Cystic Fibrosis Foundation. For more information visit www.ArcturusRx.com. In addition, please connect with us on Twitter and LinkedIn.
SOURCE: Arcturus Therapeutics
Post Views: 73
