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GNMX

Aevi Genomics Medicine

$2.21

-3.23 (-59.38%)

06:30
03/21/17
03/21
06:30
03/21/17
06:30

Aevi Genomics Medicine downgraded to Hold from Buy at Jefferies

Jefferies analyst Matthew Andrews downgraded Aevi Genomics Medicine to Hold after AEVI-001 didn't achieve significance on primary endpoint in ADHD. The analyst sees shares being range-bound and cut his price target for the stock to $2.50 from $10.

  • 21

    Mar

GNMX Aevi Genomics Medicine
$2.21

-3.23 (-59.38%)

01/05/17
JEFF
01/05/17
NO CHANGE
JEFF
Celgene, Alkermes among Jefferies' top 2017 Biotech picks
Jefferies' Biotechnology equity research team laid out their top picks for 2017. Following a volatile two years, the biotech space seeks to achieve "greater equilibrium" in 2017, the analysts write in a research note. They cite increasing competition, slowing volumes, and ramping payer leverage as reasons to remain selective when picking stocks this year and beyond. Among large-caps, Jefferies likes Celgene (CELG) for its "best-in-class growth" and sees limited downside in Gilead (GILD) shares. In the mid-cap space, the firm favors Alkermes (ALKS) given the prospects for Vivitrol and Aristada and a "strong" neurology pipeline as well as Vertex (VRTX). Jefferies' top small-cap picks include Aevi Genomics Medicine, Alder Biopharmaceuticals (ALDR), AMAG Pharmaceuticals (AMAG), DBV Technologies (DBVT), Immunomedics (IMMU), Ignyta (RXDX), Karyopharm (KPTI), RA Pharmaceuticals (RARX), TherapeuticsMD (TXMD) and Xenon Pharmaceuticals (XENE).
02/22/17
JMPS
02/22/17
INITIATION
JMPS
Outperform
Aevi Genomics Medicine coverage assumed with an Outperform at JMP Securities
JMP Securities analyst Jason Butler assumed coverage of Aevi Genomics Medicine with an $8 price target and an Outperform rating.
03/20/17
PIPR
03/20/17
NO CHANGE
Target $7
PIPR
Overweight
Aevi Genomics Medicine price target lowered to $7 from $14 at Piper Jaffray
Piper Jaffray analyst Edward Tenthoff lowered his price target on Aevi Genomics Medicine to $7 from $14 after the company announced that a trial of AEVI-001 in adolescents with ADHD did not meet the primary endpoint of the study. However, the Phase 3 trial showed a numerical improvement on the primary endpoint and a pre-specified sub-group analysis showed 30% or greater ADHD-RS-5 improvement, which he believes shows activity of AEVI-001. The analyst, who expects Aevi to conduct a longer Phase 2 study in younger patients at higher doses, pushed out his expectation for AEVI-001 approval by one year to 2021 and keeps an Overweight rating on the stock.

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