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3 Promising Penny Stocks In The US With Market Caps Under $400M

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As the U.S. stock market reaches record highs, with indices like the S&P 500 and Dow Jones posting their biggest monthly gains of 2024, investors are exploring opportunities beyond well-known large-cap stocks. Penny stocks, often representing smaller or newer companies, continue to intrigue investors despite their vintage name. This article will spotlight several penny stocks that stand out for their financial strength and potential for long-term success amidst current market conditions.

Top 10 Penny Stocks In The United States

Name

Share Price

Market Cap

Financial Health Rating

BAB (OTCPK:BABB)

$0.80

$5.81M

★★★★★★

Inter & Co (NasdaqGS:INTR)

$4.62

$2.03B

★★★★☆☆

QuantaSing Group (NasdaqGM:QSG)

$3.08

$136.98M

★★★★★★

Golden Growers Cooperative (OTCPK:GGRO.U)

$4.50

$69.71M

★★★★★★

ZTEST Electronics (OTCPK:ZTST.F)

$0.2408

$8.86M

★★★★★★

Permianville Royalty Trust (NYSE:PVL)

$1.59

$52.47M

★★★★★★

PHX Minerals (NYSE:PHX)

$3.81

$142.8M

★★★★★☆

Zynerba Pharmaceuticals (NasdaqCM:ZYNE)

$1.30

$65.6M

★★★★★☆

CBAK Energy Technology (NasdaqCM:CBAT)

$0.9429

$84.8M

★★★★★☆

Safe Bulkers (NYSE:SB)

$3.87

$413.23M

★★★★☆☆

Click here to see the full list of 709 stocks from our US Penny Stocks screener.

Below we spotlight a couple of our favorites from our exclusive screener.

Alpha Tau Medical

Simply Wall St Financial Health Rating: ★★★★★☆

Overview: Alpha Tau Medical Ltd. is a clinical-stage oncology therapeutics company focused on the research, development, and commercialization of diffusing alpha-emitters radiation therapy (Alpha DaRT) for treating solid cancers in Israel and the United States, with a market cap of approximately $195.79 million.

Operations: There are no reported revenue segments for this clinical-stage oncology therapeutics company.

Market Cap: $195.79M

Alpha Tau Medical Ltd., a pre-revenue clinical-stage oncology company, is focused on advancing its Alpha DaRT technology for treating solid cancers. Despite reporting a net loss of US$22.27 million for the first nine months of 2024, the company has made significant strides in regulatory progress and clinical trials. It was accepted into the FDA's Total Product Life Cycle Advisory Program to expedite market access for its treatment targeting recurrent glioblastoma multiforme. Additionally, it initiated clinical trials for lung cancer and received FDA approval to study recurrent cutaneous Squamous Cell Carcinoma in immunocompromised patients, highlighting potential growth avenues.