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Cidara Therapeutics Inc

Cidara Therapeutics Inc

CDTX
$221.38USD+0.03%+0.06 today

MARKET CAP

7.0B

P/E (TTM)

FWD P/E

DAY RANGE

$221 – $221

52W RANGE

$15
$221

The case for & against

Bull & Bear analysis

Bullish

Cidara Therapeutics, Inc. (NASDAQ: CDTX) is a clinical-stage biotechnology company focused on developing novel drug antibody conjugates to address significant unmet medical needs in the prevention and treatment of influenza, particularly in high-risk populations. Cidara's lead asset, CD388, aims to revolutionize the flu prevention landscape by providing a universal antiviral alternative, mitigating the limitations of current vaccines. As it progresses toward pivotal Phase III trials, Cidara stands at the forefront of a critical and evolving healthcare market.

Bull says

  • Analysts rate CDTX 'Buy' with $7-9B peak revenue potential for CD388
  • Breakthrough Therapy designation offers expedited FDA review and guidance
  • Accelerated Phase III plan targets market entry by 2026
  • $476M cash runway supports trials; potential BARDA funding boosts liquidity
  • CD388 addresses >20M high-risk patients, with expansion into broader populations
  • Proprietary Cloudbreak platform positions CD388 as a universal flu antiviral

Bear says

  • No approved products and negative earnings (P/E –18.8) fuel cash-burn concerns
  • Significant FDA approval risks; trial-design alignment may delay Phase III start
  • Dependence on BARDA grants for manufacturing scaling adds funding uncertainty
  • Vaccine competition and low flu vaccination rates could hinder CD388 uptake
  • Market cap ~$345M vs. high R&D spend increases dilution risk
  • Commodity perception of flu therapeutics may limit premium pricing

Investment themes with CDTX

Biotech +0.07%

Genetic and drug innovations driving medical breakthroughs

ABBV · AMGN · TMO

Earnings Call · Q1 2025 · Mgmt. Guidance

Updated 09-08-2026bullish

Transcript signals

Bull points

  • we see a substantial opportunity in that high-risk comorbid as well as the immune-compromised populations.
  • we expect to announce top-line data by the end of June.
  • Dependent on the results of our Phase IIb study and our regulatory discussions, we expect to initiate a Phase III study in the spring of 2026 in the southern hemisphere.

Bear points

  • the higher than expected breakthrough infection rates here?
Read full transcript analysis ›