Analyst Ratings January 23, 2026

H.C. Wainwright Elevates Corcept Therapeutics Price Target to $105 Following Positive ROSELLA Trial Outcomes

Strong Phase 3 Data for Relacorilant Boosts Valuation and Expectations Ahead of FDA Review

By Maya Rios CORT
H.C. Wainwright Elevates Corcept Therapeutics Price Target to $105 Following Positive ROSELLA Trial Outcomes
CORT

H.C. Wainwright upgraded its price target for Corcept Therapeutics to $105 from $90, maintaining a Buy rating based on encouraging results from the Phase 3 ROSELLA study evaluating relacorilant in platinum-resistant ovarian cancer. The trial demonstrated a significant improvement in overall survival when relacorilant was combined with nab-paclitaxel, with a favorable safety profile and consistent benefit regardless of biomarker status. These clinical advancements contribute to positive commercial prospects preceding a planned July 2026 FDA action date.

Key Points

  • H.C. Wainwright increased Corcept Therapeutics’ price target to $105 from $90 following positive Phase 3 data for relacorilant in platinum-resistant ovarian cancer.
  • The ROSELLA trial showed a 35% reduction in all-cause mortality when relacorilant was combined with nab-paclitaxel, extending median overall survival to 16.0 months compared to 11.9 months with chemotherapy alone.
  • Corcept plans to support a commercial launch with 50 oncology-focused sales staff, forecasting sales growth from $190 million in 2026 to $2.1 billion by 2031, with an FDA decision expected by July 2026.

Investment firm H.C. Wainwright has revised its price target on Corcept Therapeutics (NASDAQ:CORT) upward to $105 from its previous $90, while reaffirming a Buy recommendation on the stock. This adjustment follows the announcement on January 22 of promising median overall survival data emerging from Corcept's Phase 3 ROSELLA trial assessing relacorilant in combination with nab-paclitaxel for patients with platinum-resistant ovarian cancer.

The ROSELLA study revealed that participants treated with relacorilant plus nab-paclitaxel achieved a median overall survival of 16.0 months, surpassing the 11.9 months observed in the control group receiving only nab-paclitaxel. This corresponds to a 35% reduction in the risk of death from any cause, supported by a hazard ratio of 0.65 and a statistically significant p-value of 0.0004. Importantly, the safety profile of relacorilant was consistent with that of the control arm, exhibiting no additional chemotherapy-related toxicities, underscoring the treatment's tolerability.

H.C. Wainwright emphasized that, unlike many competitor therapies, the ROSELLA trial enrolled patients irrespective of biomarker expressions, with positive survival outcomes evident across various subpopulations. The firm views these results as encouraging indicators ahead of Corcept’s Prescription Drug User Fee Act (PDUFA) target date slated for July 11, 2026.

In anticipation of commercial launch, should relacorilant gain approval, Corcept intends to deploy a focused sales force comprising 50 oncology-dedicated representatives. Projected revenues are forecasted to escalate from $190 million in 2026 to approximately $2.1 billion by 2031, according to H.C. Wainwright’s analysis.

While the recent clinical progress offers strong momentum, Corcept has previously encountered regulatory headwinds. The U.S. Food and Drug Administration (FDA) issued a Complete Response Letter concerning relacorilant’s application for the treatment of hypercortisolism in Cushing’s syndrome, resulting in prior downward revisions of price targets by both H.C. Wainwright and Canaccord Genuity. Nonetheless, based on robust clinical efficacy and safety data from the ovarian cancer indication, both investment firms have maintained their Buy ratings, with Canaccord slightly raising its target to $100 after an earlier cut.

Risks

  • Regulatory risks remain relevant due to the FDA’s previous Complete Response Letter for relacorilant’s use in Cushing’s syndrome, which could affect investor sentiment and stock valuation.
  • Clinical outcomes observed in the Phase 3 study, while promising, may not guarantee approval or commercial success in other indications or broader patient populations.
  • Market competition and uncertainty in reimbursement dynamics could impact Corcept’s ability to achieve projected sales growth in the oncology sector.

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