Alzamend Neuro, Inc. ALZN

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Price alert · ALZN

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1.21 USD -0.01 -0.82%

At close · Oct 30

1.21 0.00 0.00%

After hours · Oct 30, 4:00 PM ET

Bid
1.21 × 2
Ask
1.25 × 2
1.21 Day range 1.33
0.858 52-week range 2.61
YTD
-33.52%
1 year
-53.64%
Open
1.29
Prev close
1.22
Mkt cap
5.84M
Vol
25.03K
Avg vol
79.67K
EPS
-2.30
P/E
0.00
Div yield
0.00%
More statistics
Low
1.21
High
1.33
Forward P/E
-0.26
Beta
-0.04
Short ratio
1.03
Inst. own
0.94%
Dividend
0.00
Ex-div date
Earnings
Sep 11, 2024
50-d avg
1.42
200-d avg
4.08
1y target
32.00

5D chart

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Interval

Signals (16)
NameTimeAgo
SMA: BearishOct 30, 3:25 PM2 days ago
SMA: BullishOct 30, 1:00 PM2 days ago
SMA: BullishOct 30, 12:20 PM2 days ago
SMA: BearishOct 30, 11:50 AM2 days ago
SMA: BearishOct 30, 10:35 AM2 days ago
SMA: BullishOct 30, 10:10 AM2 days ago
MACD: Sell SignalOct 29, 1:25 PM3 days ago
SMA: BearishOct 29, 1:05 PM3 days ago
MACD: Buy SignalOct 29, 9:35 AM3 days ago
SMA: BullishOct 28, 3:40 PM4 days ago
SMA: BearishOct 28, 3:20 PM4 days ago
MACD: Sell SignalOct 28, 3:20 PM4 days ago
SMA: BearishOct 28, 2:30 PM4 days ago
SMA: BearishOct 27, 2:45 PM5 days ago
SMA: BullishOct 27, 1:50 PM5 days ago
SMA: BearishOct 27, 12:10 PM5 days ago

Discussion (4)

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VICKY HANUKA ALZN 3 years ago #2

23/10/2023 08:00AM ET
Alzamend Neuro Submits IND Application for a Phase IIA Clinical Trial in Major Depressive Disorder Patients of its Next‑Generation Lithium Therapeutic Drug Candidate AL001
Safety aspects of AL001 development may qualify for a 505(b)(2) NDA pathway for FDA approval
Alzamend recently completed a Phase IIA Study of AL001 in Alzheimer's patients and healthy subjects showing a benign safety/ tolerability profile while characterizing dosing levels unlikely to require therapeutic drug monitoring
Alzamend Neuro, Inc. (NASDAQ:ALZN) ("Alzamend"), a clinical-stage biopharmaceutical company focused on developing novel products for the treatment of Alzheimer's disease ("Alzheimer's"), bipolar disorder ("BD"), major depressive disorder ("MDD") and post-traumatic stress disorder ("PTSD"), today announced that it has submitted an investigational new drug ("IND") application to the U.S. Food and Drug Administration ("FDA") for the initiation of study AL001-MDD01, a Phase IIA plasma/brain pharmacokinetics clinical study of AL001 for adjunctive treatment of patients with MDD.