Analysts Predict Up to ~450% Surge for These 2 ‘Strong Buy’ Penny Stocks

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Some of the market’s biggest winners start off as the smallest players. While trillion-dollar tech giants like the ‘Magnificent 7’ dominate the spotlight, the real hidden opportunities often lie in lesser-known stocks trading for $5 or less.

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These low-cost shares – penny stocks – may be cheap, but their potential can be massive. Many operate at the cutting edge of their industries, and when they hit the right catalyst – be it a breakthrough innovation or a disruptive product – their share prices can skyrocket.

Of course, not every penny stock is a hidden gem; some trade at low levels for a reason, struggling with poor fundamentals or challenges that may be too big to overcome.

So, how can investors spot those poised to go from rags to riches? By turning to Wall Street pros.

Using TipRanks’ database, we pinpointed two compelling penny stocks that have won over analysts, earning a ‘Strong Buy’ consensus rating. Both tickers also present strong upside potential, with one poised for a nearly 450% surge. Let’s see why they are drawing plaudits across the board.

Solid Biosciences (SLDB)

We’ll start with Solid Biosciences, a biotech research firm focused on advancing gene therapy for severe neuromuscular and cardiac diseases – areas with limited treatment options. The company is developing a gene therapy pipeline to address high unmet medical needs, including Duchenne muscular dystrophy, Friedreich’s ataxia (FA), catecholaminergic polymorphic ventricular tachycardia (CPVT), TNNT2-mediated dilated cardiomyopathy, and BAG3-mediated dilated cardiomyopathy.

At the heart of its innovation is SGT-003, a next-generation genetic therapy for Duchenne muscular dystrophy. This leading drug candidate is currently undergoing Phase I/II clinical testing in the INSPIRE DUCHENNE trial. With the first patients already receiving doses, Solid is gearing up for potential Phase 3 activities – pending results from ongoing trials. Investors eagerly anticipate the first-in-human data for SGT-003, which is expected this quarter and could mark a pivotal moment for the company’s gene therapy ambitions.

Apart from Duchenne, Solid is also advancing SGT-212, a recombinant AAV-based gene replacement therapy targeting Friedreich’s ataxia. This novel treatment is designed to deliver frataxin through two strategic routes – an intradentate nucleus (IDN) infusion using an MRI-guided device, followed by an intravenous (IV) infusion. Last month, the FDA not only granted IND clearance for clinical testing but also awarded Fast Track designation. Looking ahead, Solid plans to initiate a Phase 1b clinical trial for FA treatment in the second half of 2025.