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Harpoon Therapeutics, Inc. - HARP STOCK NEWS

Welcome to our dedicated page for Harpoon Therapeutics news (Ticker: HARP), a resource for investors and traders seeking the latest updates and insights on Harpoon Therapeutics stock.

Harpoon Therapeutics, Inc. (NASDAQ: HARP) is a clinical-stage immunotherapy company founded in 2015. Specializing in developing T cell engagers, Harpoon harnesses the body’s immune system to combat cancer and other serious diseases. Co-founded by Patrick Bauerle and Luke Evnin, the company leverages groundbreaking T cell recruiting antibodies to develop next-generation therapies. Harpoon's innovative platforms include the Tri-specific T cell Activating Construct (TriTAC®), ProTriTAC™, and TriTAC-XR. The TriTAC® platform aims to direct a patient's own immune cells to target and destroy tumor cells, primarily focusing on solid tumors and hematologic malignancies.

One of Harpoon's leading projects is HPN328, targeting delta-like ligand 3 (DLL3). Currently in a Phase 1/2 clinical trial, HPN328 shows promise in treating small cell lung cancer (SCLC) and other neuroendocrine tumors. Interim results indicate a 35% confirmed response rate in all tumor types studied, with higher efficacy observed in non-SCLC neuroendocrine tumors.

Harpoon's innovative approach extends to their proprietary ProTriTAC™ platform, which remains inactive until reaching the tumor, ensuring higher precision and reduced side effects. Additionally, the TriTAC-XR platform is designed to mitigate cytokine release syndrome, a common challenge in T cell therapies.

Financially, Harpoon has secured robust funding through recent PIPE financings, ensuring a solid runway into 2026. Strategic partnerships with leading oncology research centers and a strong focus on regulatory milestones underscore Harpoon's commitment to advancing cancer treatment. For more information, visit www.harpoontx.com.

  • HPN328 received Orphan Drug Designation from the FDA in March 2022.
  • The company is actively presenting data at major oncology conferences such as ESMO and ASCO-GU.
  • Harpoon plans to meet with regulators in early 2024 to discuss further development plans for HPN328.
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Harpoon Therapeutics, a clinical-stage immuno-oncology company, announced its participation in the virtual SVB Securities Global Biopharma Conference on February 14, 2023, at 1:40 p.m. ET. The presentation will highlight the company's innovative T cell engagers developed through its proprietary TriTAC platform, aimed at treating cancer and other diseases. A live audio webcast of the presentation will be accessible on Harpoon's website, with an archived version available afterward. For more information about Harpoon's platforms and treatments, visit www.harpoontx.com.

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Harpoon Therapeutics (HARP) presented interim results from a Phase 1 clinical trial of HPN217 for relapsed/refractory multiple myeloma at the ASH Annual Meeting. The trial involved 62 patients and showed a 77% objective response rate at the highest doses (12 and 24 mg). Many patients experienced durable responses, with 86% remaining on treatment. Low-grade cytokine release syndrome occurred in 29% of patients, with no Grade 3 events reported. Ongoing dose optimization is in progress, and the management plans to discuss these results in a conference call on December 12, 2022.

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Harpoon Therapeutics, a clinical-stage immunotherapy firm, will host a conference call on December 12, 2022, at 4:30 p.m. ET to discuss updated interim results from its Phase 1 HPN217 clinical program, presented at the 64th American Society of Hematology Annual Meeting. Interested parties can join via phone or through a webcast on Harpoon's investor relations website. The company focuses on developing innovative T cell engagers using proprietary technology to treat cancer and other diseases, with initiatives aimed at solid tumors and hematologic malignancies.

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Harpoon Therapeutics (HARP) provided a strategic update, focusing on ongoing clinical programs HPN217, HPN328, and HPN601. Following a corporate restructuring, 45% of the workforce will be reduced to cut operating expenses, with current cash of $66.1 million expected to fund operations through 2023. Q3 2022 revenue increased to $13.6 million compared to $4.5 million last year, driven by R&D collaborations. However, R&D expenses rose to $21 million, contributing to a net loss of $11.6 million. Upcoming milestones include data presentations at ASH 2022 and continued patient enrollment for clinical trials.

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Harpoon Therapeutics (HARP) announced updated interim results from its Phase 1 clinical trial of HPN217 targeting relapsed/refractory multiple myeloma, to be presented at the ASH Annual Meeting on December 11, 2022. The trial showcases clinical proof of concept for HPN217, utilizing the TriTAC platform to engage T cells against tumor cells.

The results will include safety, efficacy, and pharmacodynamic data from patients, specifically at higher dose levels, highlighting the potential of HPN217 in oncology therapeutics.

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Harpoon Therapeutics announces the appointment of Dr. Luke Walker, M.D., as the new Chief Medical Officer, effective October 3, 2022. Dr. Walker, previously with Seagen, will spearhead clinical development efforts for the company’s innovative T cell engager platforms. His extensive background includes key leadership roles in oncology drug development, notably overseeing the approval process for TUKYSA. The company also granted Dr. Walker a stock option to purchase 305,000 shares at $1.08 per share, vesting over four years.

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Harpoon Therapeutics has appointed Lauren Silvernail to its Board of Directors and as the Chairperson of its Audit Committee. Silvernail, an industry veteran with over 30 years of financial leadership experience in life sciences, previously served in significant roles at Evolus, Revance Therapeutics, and Allergan. CEO Julie Eastland expressed confidence in Silvernail's expertise to guide the company's clinical development and business strategy. Harpoon focuses on novel T cell engagers for cancer treatment, leveraging its proprietary platforms to enhance therapeutic efficacy.

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Harpoon Therapeutics (NASDAQ: HARP) announced its participation in three investor conferences in September 2022. These include one-on-one meetings at Citi's 17th Annual BioPharma Conference on September 8, a corporate presentation at H.C. Wainwright's Global Investment Conference on September 12 at 11:30 a.m. ET, and a session at Baird’s 2022 Global Healthcare Conference on September 13 at 4:20 p.m. ET. Presentations will be accessible on Harpoon's website, along with archived replays.

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Harpoon Therapeutics (HARP) presented positive interim results for HPN328 at the ASCO Annual Meeting, addressing neuroendocrine cancers with a favorable safety profile. Financially, Q2 2022 saw revenues increase to $8.3 million, attributed mainly to a Development Option Agreement with AbbVie. However, cash reserves declined to $90.2 million from $136.6 million, extending funding into H2 2023. R&D expenses rose to $20.7 million, while net loss was $17.4 million for the quarter. Leadership changes include the departure of CFO Georgia Erbez, who will assist as a consultant.

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Harpoon Therapeutics (NASDAQ: HARP), a clinical-stage immunotherapy company, announced its participation in two investor conferences. The first is a panel discussion at the Wedbush PacGrow Healthcare Conference on August 9, 2022, at 2:20 p.m. ET, focusing on immuno-oncology. The second is a corporate presentation at the Canaccord Genuity 42nd Annual Growth Conference in Boston on August 10, 2022, at 12 p.m. ET. A live audio webcast of the Canaccord presentation will be available on the Harpoon website.

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FAQ

What is the market cap of Harpoon Therapeutics (HARP)?

The market cap of Harpoon Therapeutics (HARP) is approximately 492.3M.

What is Harpoon Therapeutics' primary focus?

Harpoon Therapeutics focuses on developing novel T cell engagers to harness the body’s immune system to treat cancer and other serious diseases.

What is the TriTAC® platform?

The TriTAC® platform is Harpoon's proprietary technology designed to direct a patient's T cells to target and kill tumor cells.

What are the recent clinical trial updates for HPN328?

In the Phase 1/2 trial, HPN328 showed a 35% confirmed response rate across various neuroendocrine tumor types, with promising activity and tolerability.

What does the ProTriTAC™ platform do?

ProTriTAC™ employs a prodrug concept that keeps the T cell engager inactive until it reaches the tumor, improving precision and minimizing side effects.

What is the significance of TriTAC-XR?

TriTAC-XR is designed to mitigate cytokine release syndrome, a common side effect in T cell therapies, ensuring better patient safety.

What financial steps has Harpoon taken recently?

Harpoon secured significant funding through a PIPE financing, ensuring operational funding into 2026.

What is HPN328 targeting?

HPN328 targets delta-like ligand 3 (DLL3), associated with various neuroendocrine tumors, including SCLC.

When did HPN328 receive Orphan Drug Designation?

HPN328 received Orphan Drug Designation from the FDA in March 2022.

Where can I find more information about Harpoon Therapeutics?

Additional information is available on their website at www.harpoontx.com.

What are Harpoon’s plans for HPN328 in 2024?

Harpoon plans to meet with regulators in early 2024 to discuss the next steps in the development of HPN328.

Harpoon Therapeutics, Inc.

Nasdaq:HARP

HARP Rankings

HARP Stock Data

492.35M
21.32M
0.35%
82.85%
2.52%
Biotechnology
Healthcare
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United States
South San Francisco