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CASI News
CASI Events
Casi Pharmaceuticals Receives Nasdaq Delisting Notice
Casi Pharmaceuticals announced that it has received a determination letter from the hearings panel of the Nasdaq Stock Market dated February 23, notifying the company that the panel determined to delist the company's securities from Nasdaq, due to the company's failure to satisfy the continued listing conditions as previously disclosed. As a result, the company securities will be suspended from trading at the open of business on February 26, and delisted from Nasdaq after the completion of certain applicable process. The company does not intend to request a review of such decision. Following the delisting, the company expects that its ordinary shares will be quoted on the "over the counter" market operated by OTC Markets Group Inc. so that a trading market may continue to exist for its ordinary shares. The delisting from Nasdaq will have no significant impact on the company's operations.
CASI Pharmaceuticals Determined for Delisting by Nasdaq
CASI Pharmaceuticals received a determination letter from the Hearings Panel of The Nasdaq Stock Market dated February 23, 2026, notifying the Company that the Panel determined to delist the Company's securities from Nasdaq, due to the Company's failure to satisfy the continued listing conditions as previously disclosed. As a result, the Company securities will be suspended from trading at the open of business on February 26, 2026, and delisted from Nasdaq after the completion of certain applicable process. The Company does not intend to request a review of such decision.Following the delisting, the Company expects that its ordinary shares will be quoted on the "over the counter" market operated by OTC Markets Group so that a trading market may continue to exist for its ordinary shares.
CASI Pharmaceuticals Approved for CID-103 Clinical Trial
CASI Pharmaceuticals announced that China National Medical Products Administration has approved a Clinical Trial Application to conduct a Phase 1 /2 clinical trial for CID-103 in adults with chronic active renal allograft antibody-mediated rejection. The Phase 1 / 2 clinical trial is a dose-ranging and safety study evaluating the tolerability and efficacy of CID-103 in patients with renal allograft AMR.
CASI Pharmaceuticals Announces CID-103 Update, Acquisition Proposal at $1.15 per Share
CASI Pharmaceuticals announced additional data from its Phase 1 open-label study of CID-103 in adult patients with immune thrombocytopenia. Initial clinical data from this study were presented at the 67th American Society of Hematology Annual Meeting and Exposition on December 7, 2025, in Orlando, Florida. Updated safety and efficacy data can be found on the CASI website here. The update includes additional safety and efficacy data based on: CID-103 at 30 mg, 150 mg, 300 mg, 600 mg and 900 mg; ~5 weeks of additional dosing / follow up for the ongoing patients in all cohorts; 3 additional patients enrolled in 900 mg cohort; 2 patients are at Week 5 of study treatment; 1 patient is at Week 3 of study treatment; 2 additional patients enrolled and one patient is in screening in 600 mg cohort; 1 patient is at Week 3 of study treatment; 1 patient is at Week 2 of study treatment. Interim Results: CID-103 demonstrated a manageable safety profile with only two Grade 3 treatment-related events and no dose limiting toxicities observed; All infusion-related reactions occurred with priming dose and are due to low grade AEs; Primary Efficacy Endpoint achieved in 12 of 15 evaluable patients; 10 of 15 evaluable patients achieved Complete Response with platelet improvement observed as early as one week post dose; Reduction of PD markers (decreased anti-platelet antibodies, immunoglobulins, NK and plasma cells) is consistent with the presumed CID-103 MOA resulting in the observed platelet response Separately, the Company announced that its board of directors received a preliminary non-binding proposal, dated January 7, 2026,which was further amended by an updated preliminary non-binding proposal dated January 9, 2026 from Dr. Wei-Wu He, to acquire all of the outstanding ordinary shares, par value $0.0001 per share, of the Company, that are not already beneficially owned by Dr. He for a proposed purchase price of $1.15 per Ordinary Share. The proposed price represents a 30% premium to the average closing price during the last 30 trading days.
CASI Pharmaceuticals Enters $20 Million Convertible Note Agreement with ETP Global
CASI Pharmaceuticals announced that the Company has entered into a convertible note purchase agreement with ETP Global III Fund LP, a partnership controlled by Dr. Wei-Wu He, pursuant to which the Company will issue and sell convertible notes in an aggregate principal amount of US $20 million to the Purchaser through a private placement. This investment is planned to provide runway to fund the Company through a Phase 1 study in China in renal allograft anti-body-mediated rejection as well as development toward a stable, high concentration protein solution for subcutaneous formulation.
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