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Poseida Therapeutics, Inc. Stock Price

NasdaqGS:PSTX Community·US$934.7m Market Cap
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PSTX Share Price Performance

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Snowflake Analysis

Excellent balance sheet and fair value.

3 Risks
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Poseida Therapeutics, Inc. Key Details

US$150.9m

Revenue

US$172.4m

Cost of Revenue

-US$21.6m

Gross Profit

US$39.2m

Other Expenses

-US$60.8m

Earnings

Last Reported Earnings
Sep 30, 2024
Next Reporting Earnings
n/a
-0.62
-14.30%
-40.28%
67.5%
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About PSTX

Founded
2014
Employees
350
CEO
Kristin Yarema
WebsiteView website
poseida.com

Poseida Therapeutics, Inc., a clinical-stage biopharmaceutical company, focuses on developing therapeutics for patients with high unmet medical needs. The company’s development candidates for Heme Malignancies includes P-BCMA-ALLO1, which is in Phase I trial to treat patients with relapsed/refractory multiple myeloma; P-CD19CD20-ALLO1, which is in Phase I trial for treating B cell malignancies and other autoimmune diseases; P-BCMACD19-ALLO1, an allogeneic, off-the-shelf CAR-T product candidate in preclinical development for treating multiple myeloma; and P-CD70-ALLO1 under preclinical development to treat hematological indications. It is also involved in the development of P-MUC1C-ALLO1 that is in Phase I trial for treating a range of solid tumors, including breast, colorectal, lung, ovarian, pancreatic, and renal cancers; P-PSMA-ALLO1, an autologous chimeric antigen receptor T cell (CAR-T) product candidate that is in preclinical development for the treatment of patients with metastatic castrate resistant prostate cancer (mCRPC); and P-PSMA-101, an allogeneic CAR-T product candidate under Phase 1 clinical trial for treating mCRPC. In addition, the company engages in the development of P-FVIII-101, a clinical stage liver-directed gene therapy for the in vivo treatment of hemophilia A; P-OTC-101, a clinical stage liver-directed gene therapy for the in vivo treatment of ornithine transcarbamylase deficiency; and P-PAH-101, a clinical stage liver-directed gene therapy for the in vivo treatment of phenylketonuria. It has a research collaboration and license agreement with F. Hoffmann-La Roche Ltd, and Hoffmann-La Roche Inc. The company was incorporated in 2014 and is headquartered in San Diego, California.

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