We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies, revised Privacy Policy and Terms of Service.
You are being directed to ZacksTrade, a division of LBMZ Securities and licensed broker-dealer. ZacksTrade and Zacks.com are separate companies. The web link between the two companies is not a solicitation or offer to invest in a particular security or type of security. ZacksTrade does not endorse or adopt any particular investment strategy, any analyst opinion/rating/report or any approach to evaluating individual securities.
If you wish to go to ZacksTrade, click OK. If you do not, click Cancel.
Avidity (RNA) Down on Update From Neuromuscular Disease Study
Read MoreHide Full Article
Avidity Biosciences, Inc. (RNA - Free Report) provided an update on its phase I/II study of AOC 1001 in adults with myotonic dystrophy type I (DM1). The company reported that it is engaged in ongoing discussions with the FDA regarding the partial clinical hold on new participant enrollment in the MARINA study. The company continues to share new AOC 1001 data with the regulatory body as it emerges from the MARINA study. However, the stock of the company dropped about 17% on Thursday, following the company’s decision to conclude the MARINA study with the 38 participants enrolled at 1 mg/kg, 2 mg/kg and 4 mg/kg of AOC 1001 and will not move forward with the 8 mg/kg dose of AOC 1001.
AOC 1001, Avidity’s lead product candidate, is part of the company’s new class of RNA therapy candidates called Antibody Oligonucleotide Conjugates (AOC). The mechanism of action of AOC 1001 includes a proprietary monoclonal antibody that binds to the transferrin receptor 1 (TfR1) conjugated with a siRNA targeting DMPK mRNA.
In the past year, shares of Avidity have declined 16% compared with the industry’s 14.3% fall.
Image Source: Zacks Investment Research
DM1 is a rare, progressive, neuromuscular disease with an extremely high mortality rate. DM1 primarily affects skeletal and cardiac muscles. However, it can cause a plethora of complexities, like myotonia and muscle weakness, respiratory problems, fatigue, hypersomnia, cardiac abnormalities, severe gastrointestinal complications and cognitive and behavioral impairment.
We would like to remind the investors that in September 2022, a partial clinical hold was issued by the FDA on new participant enrollment in Avidity’s phase I/II MARINA study. This partial hold was the consequence of a serious complexity reported in a single participant in the 4 mg/kg cohort of the MARINA study. The study investigator then concluded that the adverse event was related to the AOC 1001. However, post thorough analysis, Avidity reported that the unfortunate occurrence was a result of an unforeseen rare complication without a plausible biological link to any component of AOC 1001, the AOC platform, the transferrin receptor delivery mechanism or the reduction of DMPK. The company emphasized the fact that AOC 1001 does not cross the blood-brain barrier.
In December 2022, the company reported positive data from a preliminary assessment of the phase I/II MARINA study of AOC 1001. Data showed that the mechanism of action was successfully carried out with early signs of clinical activity with improvement in myotonia after just one or two doses of the candidate. Data from the preliminary assessment reportedly supports that the targeted dose range is between 2 mg/kg and 4 mg/kg of AOC 1001.
Following these findings, Avidity also announced its decision to continue dosing in both the patient cohorts, receiving 2 mg/kg and 4 mg/kg of AOC 1001 in the MARINA-OLE study. The study will evaluate the long-term safety and tolerability of AOC 1001 in participants with DM1 who were previously enrolled in the MARINA phase I/II study. The company expects to share top-line data from the study toward the end of 2023.
Management is focused on resolving the partial clinical hold and remains confident about AOC 1001’s benefit/risk profile.
In the past 90 days, the Zacks Consensus Estimate for Aptinyx’s 2023 loss per share has narrowed from 77 cents to 56 cents. In the past year, shares of Aptinyx have fallen by 94.2%.
APTX beat estimates in each of the trailing four quarters, delivering an average earnings surprise of 9.53%.
In the past 90 days, the consensus estimate for Annovis’ 2023 loss per share has narrowed from $2.94 to $2.93. In the past year, shares of Annovis have increased by 45.4%.
ANVS’ reported loss per share was narrower than the estimated loss per share in the last reported quarter, delivering an earnings surprise of 20.51%.
In the past 90 days, the consensus estimate for ADMA’s 2023 loss per share has narrowed from 20 cents to 14 cents. In the past year, shares of ADMA have increased by 66.4%.
ADMA beat estimates in three out of the trailing four quarters, delivering an average earnings surprise of 2.88%.
See More Zacks Research for These Tickers
Normally $25 each - click below to receive one report FREE:
Image: Bigstock
Avidity (RNA) Down on Update From Neuromuscular Disease Study
Avidity Biosciences, Inc. (RNA - Free Report) provided an update on its phase I/II study of AOC 1001 in adults with myotonic dystrophy type I (DM1). The company reported that it is engaged in ongoing discussions with the FDA regarding the partial clinical hold on new participant enrollment in the MARINA study. The company continues to share new AOC 1001 data with the regulatory body as it emerges from the MARINA study. However, the stock of the company dropped about 17% on Thursday, following the company’s decision to conclude the MARINA study with the 38 participants enrolled at 1 mg/kg, 2 mg/kg and 4 mg/kg of AOC 1001 and will not move forward with the 8 mg/kg dose of AOC 1001.
AOC 1001, Avidity’s lead product candidate, is part of the company’s new class of RNA therapy candidates called Antibody Oligonucleotide Conjugates (AOC). The mechanism of action of AOC 1001 includes a proprietary monoclonal antibody that binds to the transferrin receptor 1 (TfR1) conjugated with a siRNA targeting DMPK mRNA.
In the past year, shares of Avidity have declined 16% compared with the industry’s 14.3% fall.
Image Source: Zacks Investment Research
DM1 is a rare, progressive, neuromuscular disease with an extremely high mortality rate. DM1 primarily affects skeletal and cardiac muscles. However, it can cause a plethora of complexities, like myotonia and muscle weakness, respiratory problems, fatigue, hypersomnia, cardiac abnormalities, severe gastrointestinal complications and cognitive and behavioral impairment.
We would like to remind the investors that in September 2022, a partial clinical hold was issued by the FDA on new participant enrollment in Avidity’s phase I/II MARINA study. This partial hold was the consequence of a serious complexity reported in a single participant in the 4 mg/kg cohort of the MARINA study. The study investigator then concluded that the adverse event was related to the AOC 1001. However, post thorough analysis, Avidity reported that the unfortunate occurrence was a result of an unforeseen rare complication without a plausible biological link to any component of AOC 1001, the AOC platform, the transferrin receptor delivery mechanism or the reduction of DMPK. The company emphasized the fact that AOC 1001 does not cross the blood-brain barrier.
In December 2022, the company reported positive data from a preliminary assessment of the phase I/II MARINA study of AOC 1001. Data showed that the mechanism of action was successfully carried out with early signs of clinical activity with improvement in myotonia after just one or two doses of the candidate. Data from the preliminary assessment reportedly supports that the targeted dose range is between 2 mg/kg and 4 mg/kg of AOC 1001.
Following these findings, Avidity also announced its decision to continue dosing in both the patient cohorts, receiving 2 mg/kg and 4 mg/kg of AOC 1001 in the MARINA-OLE study. The study will evaluate the long-term safety and tolerability of AOC 1001 in participants with DM1 who were previously enrolled in the MARINA phase I/II study. The company expects to share top-line data from the study toward the end of 2023.
Management is focused on resolving the partial clinical hold and remains confident about AOC 1001’s benefit/risk profile.
Avidity Biosciences, Inc. Price and Consensus
Avidity Biosciences, Inc. price-consensus-chart | Avidity Biosciences, Inc. Quote
Zacks Rank and Stocks to Consider
Avidity currently has a Zacks Rank #3 (Hold).
Some top-ranked stocks in the same industry are Aptinyx , Annovis Bio (ANVS - Free Report) and ADMA Biologics (ADMA - Free Report) , all carrying a Zacks Rank #2 (Buy) at present. You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.
In the past 90 days, the Zacks Consensus Estimate for Aptinyx’s 2023 loss per share has narrowed from 77 cents to 56 cents. In the past year, shares of Aptinyx have fallen by 94.2%.
APTX beat estimates in each of the trailing four quarters, delivering an average earnings surprise of 9.53%.
In the past 90 days, the consensus estimate for Annovis’ 2023 loss per share has narrowed from $2.94 to $2.93. In the past year, shares of Annovis have increased by 45.4%.
ANVS’ reported loss per share was narrower than the estimated loss per share in the last reported quarter, delivering an earnings surprise of 20.51%.
In the past 90 days, the consensus estimate for ADMA’s 2023 loss per share has narrowed from 20 cents to 14 cents. In the past year, shares of ADMA have increased by 66.4%.
ADMA beat estimates in three out of the trailing four quarters, delivering an average earnings surprise of 2.88%.