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Poseida Therapeutics Q2 2023 Earnings Report

Poseida Therapeutics logo
$9.45 +0.04 (+0.43%)
(As of 12/20/2024 05:31 PM ET)

Poseida Therapeutics EPS Results

Actual EPS
-$0.32
Consensus EPS
-$0.53
Beat/Miss
Beat by +$0.21
One Year Ago EPS
N/A

Poseida Therapeutics Revenue Results

Actual Revenue
$20.01 million
Expected Revenue
$10.00 million
Beat/Miss
Beat by +$10.01 million
YoY Revenue Growth
N/A

Poseida Therapeutics Announcement Details

Quarter
Q2 2023
Time
N/A
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Poseida Therapeutics Earnings Headlines

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About Poseida Therapeutics

Poseida Therapeutics (NASDAQ:PSTX), 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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