RAPT Therapeutics plans to report Phase 2 data on RPT904 for Chronic Spontaneous Urticaria on October 20, 2025.
Quiver AI Summary
RAPT Therapeutics, Inc. announced that it will release topline data from its Phase 2 clinical trial of RPT904 in patients with Chronic Spontaneous Urticaria (CSU) on October 20, 2025, through a press release and a webcast. This trial was conducted in partnership with Shanghai Jeyou Pharmaceutical Co., Ltd. The company will hold a conference call at 8:30 a.m. ET the same day, where participants can engage in a live Q&A session. RAPT Therapeutics specializes in developing novel therapies for inflammatory and immunological diseases. The press release also includes forward-looking statements concerning the potential outcomes and risks associated with their clinical developments and emphasizes that actual results may differ due to various uncertainties.
Potential Positives
- The announcement of topline data from the Phase 2 clinical trial of RPT904 in patients with Chronic Spontaneous Urticaria (CSU) indicates progress in the company's drug development pipeline, which is significant for investor interest and confidence.
- The upcoming webcast conference call on October 20, 2025, provides an opportunity for stakeholders to gain insights into the trial data and engage with the company directly, enhancing transparency and communication with the investment community.
Potential Negatives
- The reliance on a partner, Shanghai Jeyou Pharmaceutical Co., Ltd., for reporting clinical trial data may indicate limited control over the outcomes and timeline, which could affect investor confidence.
- The forward-looking statements indicate significant risks and uncertainties associated with the development of RPT904, including potential unfavorable safety or efficacy data that could impact regulatory approval and market viability.
- The mention of macroeconomic and geopolitical conditions that could disrupt clinical trials adds a layer of volatility that may concern investors about the stability of the company's future performance.
FAQ
What is RAPT Therapeutics announcing on October 20, 2025?
RAPT Therapeutics will report topline data from a Phase 2 clinical trial of RPT904 for Chronic Spontaneous Urticaria.
How can I join the RAPT Therapeutics conference call?
To join the call, pre-register online to receive a phone number and unique passcode for participation.
Where can I access the live webcast of the presentation?
The live webcast and audio archive will be available on the RAPT Therapeutics website.
What are RAPT Therapeutics' focus areas?
RAPT specializes in developing therapies for patients with inflammatory and immunological diseases.
What should I know about forward-looking statements in the press release?
The press release contains forward-looking statements regarding RPT904's development, potential risks, and uncertainties affecting outcomes.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$RAPT Hedge Fund Activity
We have seen 6 institutional investors add shares of $RAPT stock to their portfolio, and 46 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- MEDICXI VENTURES MANAGEMENT (JERSEY) LTD added 2,794,000 shares (+inf%) to their portfolio in Q3 2025, for an estimated $72,057,260
- TCG CROSSOVER MANAGEMENT, LLC removed 1,636,275 shares (-100.0%) from their portfolio in Q2 2025, for an estimated $13,090,200
- RTW INVESTMENTS, LP removed 1,470,500 shares (-100.0%) from their portfolio in Q2 2025, for an estimated $11,764,000
- COLUMN GROUP LLC added 1,162,536 shares (+700.0%) to their portfolio in Q2 2025, for an estimated $9,300,288
- DEEP TRACK CAPITAL, LP removed 751,423 shares (-100.0%) from their portfolio in Q2 2025, for an estimated $6,011,384
- PERCEPTIVE ADVISORS LLC removed 368,478 shares (-66.7%) from their portfolio in Q2 2025, for an estimated $2,947,824
- NANTAHALA CAPITAL MANAGEMENT, LLC added 324,997 shares (+51.9%) to their portfolio in Q2 2025, for an estimated $2,599,976
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
$RAPT Analyst Ratings
Wall Street analysts have issued reports on $RAPT in the last several months. We have seen 6 firms issue buy ratings on the stock, and 0 firms issue sell ratings.
Here are some recent analyst ratings:
- Barclays issued a "Overweight" rating on 10/13/2025
- Clear Street issued a "Buy" rating on 09/30/2025
- Leerink Partners issued a "Outperform" rating on 09/26/2025
- Wells Fargo issued a "Overweight" rating on 08/08/2025
- LifeSci Capital issued a "Outperform" rating on 07/22/2025
- HC Wainwright & Co. issued a "Buy" rating on 05/22/2025
To track analyst ratings and price targets for $RAPT, check out Quiver Quantitative's $RAPT forecast page.
$RAPT Price Targets
Multiple analysts have issued price targets for $RAPT recently. We have seen 8 analysts offer price targets for $RAPT in the last 6 months, with a median target of $33.0.
Here are some recent targets:
- Etzer Darout from Barclays set a target price of $35.0 on 10/13/2025
- Kaveri Pohlman from Clear Street set a target price of $41.0 on 09/30/2025
- Thomas Smith from Leerink Partners set a target price of $37.0 on 09/26/2025
- Eliana Merle from UBS set a target price of $9.0 on 08/12/2025
- Yanan Zhu from Wells Fargo set a target price of $38.0 on 08/08/2025
- Anupam Rama from JP Morgan set a target price of $14.0 on 07/30/2025
- An analyst from LifeSci Capital set a target price of $31.0 on 07/22/2025
Full Release
SOUTH SAN FRANCISCO, Calif., Oct. 19, 2025 (GLOBE NEWSWIRE) -- RAPT Therapeutics, Inc. (Nasdaq: RAPT), a clinical-stage immunology-based biopharmaceutical company focused on discovering, developing and commercializing novel therapies for patients living with inflammatory and immunological diseases, today announced that the Company plans to report topline data from the Phase 2 clinical trial of RPT904 (JYB1904) in patients with Chronic Spontaneous Urticaria (CSU) conducted by its partner, Shanghai Jeyou Pharmaceutical Co., Ltd. (Jeyou), formerly called Shanghai Jemincare Pharmaceutical Co., Ltd., in a premarket press release and webcast on Monday, October 20, 2025.
RAPT will host a webcast conference call accompanied by a slide presentation on
Monday, October 20, 2025 at 8:30 a.m. ET
. To join the conference call via phone and participate in the live Q&A session, please pre-register online
here
to receive a telephone number and unique passcode required to enter the call. The live webcast and audio archive of the presentation may be accessed on the RAPT Therapeutics website at
https://investors.rapt.com/events-and-presentations
.
About RAPT Therapeutics, Inc.
RAPT is a clinical-stage immunology-based biopharmaceutical company focused on discovering, developing and commercializing novel therapies for patients living with inflammatory and immunological diseases. Utilizing our deep and proprietary expertise in immunology, we develop novel therapies that are designed to modulate the critical immune responses underlying these diseases.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as “anticipate,” “estimates,” “expects,” “look forward,” “on track,” “planned,” “potential” “will” and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements. These statements relate to future events and involve known and unknown risks, uncertainties and other factors that may cause our actual results, performance or achievements to be materially different from any future performances or achievements expressed or implied by the forward-looking statements. Each of these statements is based only on current information, assumptions and expectations that are inherently subject to change and involve a number of risks and uncertainties. Forward-looking statements include, but are not limited to, statements about the development of RPT904, regulatory interactions, the therapeutic and commercial potential of RPT904, the design and timing of clinical trials and the availability of data therefrom, and other statements that are not historical fact. Many factors may cause differences between current expectations and actual results, including unexpected or unfavorable safety or efficacy data observed during clinical studies, preliminary data and trends that may not be predictive of future data or results or that may not demonstrate safety or efficacy or lead to regulatory approval, our reliance on our partners and other third parties, clinical trial site activation or enrollment rates that are lower than expected, unanticipated or greater than anticipated impacts or delays due to macroeconomic and geopolitical conditions (including the long-term impacts of ongoing overseas conflicts, tariffs and trade tensions, fluctuations in inflation and interest rates and other economic uncertainty), changes in expected or existing competition, changes in the regulatory environment, the uncertainties and timing of the regulatory approval process and the sufficiency of RAPT’s cash resources. Detailed information regarding risk factors that may cause actual results to differ materially from the results expressed or implied by statements in this press release may be found in RAPT’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2025, filed with the Securities and Exchange Commission (SEC) on August 7, 2025, and subsequent filings made by RAPT with the SEC. These forward-looking statements speak only as of the date hereof. RAPT disclaims any obligation to update these forward-looking statements, except as required by law.
RAPT Investor Contact:
Sylvia Wheeler
[email protected]
RAPT Media Contact:
Aljanae Reynolds
[email protected]