Pudu Robotics Launches PUDU T600 Series to Redefine Heavy-Payload Industrial Delivery

SHENZHEN, China, July 24, 2025 /PRNewswire/ -- Pudu Robotics, a global leader in service robotics, today announced the launch of the PUDU T600 Series, a next-generation lineup of industrial delivery robots purpose-built for high-payload, autonomous goods handling in complex industrial environments.

Following the success of the PUDU T300, which addressed mid-load transport needs, the T600 Series marks Pudu's expansion into heavy-payload logistics and end-to-end automation. It is designed to help manufacturers respond to growing demands for throughput, labor flexibility, and adaptive intralogistics—especially in fast-changing production and warehouse settings.

Dual-Form Design for Greater Application Flexibility

The T600 Series offers two distinct versions to meet varied industrial needs. The PUDU T600 is the standard version of the series—a Heavy-payload Industrial Delivery Robot, features a built-in touchscreen, ergonomic handlebar, and intuitive control buttons, enabling easy operation for tasks that require occasional manual interaction. The PUDU T600 Underride is a chassis-based industrial AMR designed with a low-profile build that allows it to autonomously navigate beneath racks or shelves, lift and transport them with precision—ideal for high-density, automated shelf-to-line or shelf-to-shelf operations.

Key Features & Innovations

• 600kg Heavy Load Capacity

With a 600kg payload capacity, the T600 Series significantly reduces the number of delivery trips required, enhancing throughput and single-trip efficiency for heavy-duty logistics operations.

• Flexible Deployment

The T600 Series is designed for fast deployment, allowing it to adapt to changing production layouts without requiring physical modifications or lengthy setup processes.

• Rack Group Recognition

Advanced navigation and perception systems enable the T600 series to intelligently identify designated shelves or cargo positions and execute autonomous pick-up and drop-off tasks—enabling fully unmanned operations in storage, delivery, and replenishment scenarios.

• Idle Elevator Prioritization for Multi-Floor Operations

To overcome elevator congestion in vertical facilities, the T600 uses a real-time scheduling system that identifies and prioritizes idle elevators, improving delivery speed and minimizing wait times during inter-floor transport.

• On-Premises Deployment for Data Security

The T600 supports on-premises or private cloud deployment, keeping data within internal networks and eliminating reliance on external cloud services—ideal for security-sensitive industrial environments.

• Adaptive Navigation in Narrow Aisles

Designed for high-density environments, the T600 Series dynamically adapts its pathing strategy based on aisle width and load dimensions, switching between single-lane or dual-lane traffic in real time to ensure safe, efficient passage and coordinated multi-robot operations.

• VDA5050 Protocol Compatibility

Support for the VDA5050 communication standard allows the T600 to seamlessly integrate with other robots and systems, simplifying fleet collaboration and scalability.

• Comprehensive Multi-Layer Safety System

The PUDU T600 Series is built for safe operation with features such as ground projection indicators (standard version) to alert nearby personnel, real-time dynamic obstacle avoidance, and an integrated disaster response module that enables automatic action during emergencies like fires or earthquakes.

• IoT-Enabled for Smarter Facility Integration

The T600's modular IoT connectivity supports access control, elevator rides, goods call buttons, and more—allowing it to quickly interface with factory systems without complex software integration.

Whether deployed in electronics assembly, automotive parts production, metal fabrication, or smart warehousing, the T600 Series is engineered to streamline logistics flows, reduce manual handling risks, and future-proof intralogistics networks through intelligent automation.

Learn more about PUDU T600 Series: https://www.pudurobotics.com/en/products/pudut600?utm_source=news&utm_medium=organic&utm_campaign=pr

About PUDU

Pudu Robotics, a global leader in the service robotics sector, is dedicated to enhancing human productivity and living standards through innovative robot technology. With a focus on R&D, manufacturing, and sales of service robots, Pudu Robotics emphasizes three core technologies: mobility, manipulation, and artificial intelligence. Pudu Robotics has taken the lead in establishing a comprehensive range of specialized, semi-humanoid, and humanoid robotic products in the industry. Currently, Pudu Robotics offers three product lines: service delivery robots, commercial cleaning robots, and industrial delivery robots, which are deployed across ten major industries, including food and beverage, retail, hospitality, healthcare, entertainment and sports, industrial facilities, education, and more. To date, Pudu Robotics has successfully shipped over 100,000 units to a variety of markets, with a presence in more than 1,000 cities across 80+ countries and regions worldwide.  For more information on business developments and updates, follow PUDU on LinkedIn, Facebook, YouTube, Twitter and Instagram.

SHENZHEN, China, July 24, 2025 /PRNewswire/ -- Pudu Robotics, a global leader in service robotics, today announced the launch of the PUDU T600 Series, a next-generation lineup of industrial delivery robots purpose-built for high-payload, autonomous goods handling in complex industrial environments.

Following the success of the PUDU T300, which addressed mid-load transport needs, the T600 Series marks Pudu's expansion into heavy-payload logistics and end-to-end automation. It is designed to help manufacturers respond to growing demands for throughput, labor flexibility, and adaptive intralogistics—especially in fast-changing production and warehouse settings.

Dual-Form Design for Greater Application Flexibility

The T600 Series offers two distinct versions to meet varied industrial needs. The PUDU T600 is the standard version of the series—a Heavy-payload Industrial Delivery Robot, features a built-in touchscreen, ergonomic handlebar, and intuitive control buttons, enabling easy operation for tasks that require occasional manual interaction. The PUDU T600 Underride is a chassis-based industrial AMR designed with a low-profile build that allows it to autonomously navigate beneath racks or shelves, lift and transport them with precision—ideal for high-density, automated shelf-to-line or shelf-to-shelf operations.

Key Features & Innovations

• 600kg Heavy Load Capacity

With a 600kg payload capacity, the T600 Series significantly reduces the number of delivery trips required, enhancing throughput and single-trip efficiency for heavy-duty logistics operations.

• Flexible Deployment

The T600 Series is designed for fast deployment, allowing it to adapt to changing production layouts without requiring physical modifications or lengthy setup processes.

• Rack Group Recognition

Advanced navigation and perception systems enable the T600 series to intelligently identify designated shelves or cargo positions and execute autonomous pick-up and drop-off tasks—enabling fully unmanned operations in storage, delivery, and replenishment scenarios.

• Idle Elevator Prioritization for Multi-Floor Operations

To overcome elevator congestion in vertical facilities, the T600 uses a real-time scheduling system that identifies and prioritizes idle elevators, improving delivery speed and minimizing wait times during inter-floor transport.

• On-Premises Deployment for Data Security

The T600 supports on-premises or private cloud deployment, keeping data within internal networks and eliminating reliance on external cloud services—ideal for security-sensitive industrial environments.

• Adaptive Navigation in Narrow Aisles

Designed for high-density environments, the T600 Series dynamically adapts its pathing strategy based on aisle width and load dimensions, switching between single-lane or dual-lane traffic in real time to ensure safe, efficient passage and coordinated multi-robot operations.

• VDA5050 Protocol Compatibility

Support for the VDA5050 communication standard allows the T600 to seamlessly integrate with other robots and systems, simplifying fleet collaboration and scalability.

• Comprehensive Multi-Layer Safety System

The PUDU T600 Series is built for safe operation with features such as ground projection indicators (standard version) to alert nearby personnel, real-time dynamic obstacle avoidance, and an integrated disaster response module that enables automatic action during emergencies like fires or earthquakes.

• IoT-Enabled for Smarter Facility Integration

The T600's modular IoT connectivity supports access control, elevator rides, goods call buttons, and more—allowing it to quickly interface with factory systems without complex software integration.

Whether deployed in electronics assembly, automotive parts production, metal fabrication, or smart warehousing, the T600 Series is engineered to streamline logistics flows, reduce manual handling risks, and future-proof intralogistics networks through intelligent automation.

Learn more about PUDU T600 Series: https://www.pudurobotics.com/en/products/pudut600?utm_source=news&utm_medium=organic&utm_campaign=pr

About PUDU

Pudu Robotics, a global leader in the service robotics sector, is dedicated to enhancing human productivity and living standards through innovative robot technology. With a focus on R&D, manufacturing, and sales of service robots, Pudu Robotics emphasizes three core technologies: mobility, manipulation, and artificial intelligence. Pudu Robotics has taken the lead in establishing a comprehensive range of specialized, semi-humanoid, and humanoid robotic products in the industry. Currently, Pudu Robotics offers three product lines: service delivery robots, commercial cleaning robots, and industrial delivery robots, which are deployed across ten major industries, including food and beverage, retail, hospitality, healthcare, entertainment and sports, industrial facilities, education, and more. To date, Pudu Robotics has successfully shipped over 100,000 units to a variety of markets, with a presence in more than 1,000 cities across 80+ countries and regions worldwide.  For more information on business developments and updates, follow PUDU on LinkedIn, Facebook, YouTube, Twitter and Instagram.

** The press release content is from PR Newswire. Bastille Post is not involved in its creation. **

Pudu Robotics Launches PUDU T600 Series to Redefine Heavy-Payload Industrial Delivery

HIGHLIGHTS

• Following an interim data review of the Cohort Expansion Phase (Phase II) of the SECuRE trial, the Safety Review Committee (SRC) confirms the trial will continue with no modifications to the protocol.

Patient population

• With the SECuRE trial continuing to recruit, a total of nine participants who had evaluable data by the 25^th of November 2025 were included in the interim assessment by the SRC, with the majority of participants receiving at least two cycles of 8 GBq of ⁶⁷Cu-SAR-bisPSMA each by the data cut-off date.
• Seven participants received ⁶⁷Cu-SAR-bisPSMA and two participants were treated with a combination of ⁶⁷Cu-SAR-bisPSMA with enzalutamide.
• Most participants were heavily pre-treated (with 55.6% having received more than 5 previous anti-cancer regimens) and had bone metastasis (66.7%).

Safety

• The safety profile of ⁶⁷Cu-SAR-bisPSMA remains favourable with most related adverse events (AEs) in the Cohort Expansion to date being Grade 1 or 2. The most common AEs were nausea and lymphopenia (observed in 33.3% of participants, for each AE).

Efficacy

• Six participants had at least two prostate specific antigen (PSA) results following ⁶⁷Cu-SAR-bisPSMA administration, with all showing a decrease in PSA. Of those, four participants (66.7%) thus far had a reduction of more than 50% in PSA (PSA50) and two participants (33.3%) had a reduction of more than 80% (PSA80).
• One participant who presented with bone metastasis at enrolment achieved undetectable PSA with no prostate cancer detected by computed tomography (CT) or bone scan following ⁶⁷Cu-SAR-bisPSMA treatment. The participant reported having excellent quality of life following the treatment.

Next Steps

• The SECuRE trial will continue enrolment into the Cohort Expansion Phase with planned completion of recruitment in 2026. Phase III registrational trial planning ongoing based on data generated to date.

SYDNEY, Jan. 15, 2026 /PRNewswire/ -- Clarity Pharmaceuticals (ASX: CU6) ("Clarity" or "Company"), a clinical-stage radiopharmaceutical company with a mission to develop next-generation products that improve treatment outcomes for patients with cancer, is pleased to share a number of updates on the SECuRE trial following an SRC meeting. The SRC has recommended that the trial continue with the Cohort Expansion Phase (Phase II) as planned with no modifications to the protocol. The interim results assessed by the SRC were collected from nine participants enrolled in the cohort that had evaluable data by the cut-off date of the 25^th of November 2025 and continue to show promising efficacy and a favourable safety profile of ⁶⁷Cu-SAR-bisPSMA.

The majority of the nine participants had bone metastasis at enrolment (66.7%) and received multiple lines of previous treatments (more than 5 previous anti-cancer regimens, 55.6%). Median PSA prior to ⁶⁷Cu-SAR-bisPSMA treatment was 18.9 ng/mL (range 1.5-30.2 ng/mL). Six out of these nine participants received at least 2 cycles of 8 GBq of ⁶⁷Cu-SAR-bisPSMA each, with two of them also receiving concomitant enzalutamide.

Of the nine participants included in this SRC analysis, six had at least two PSA results following their ⁶⁷Cu-SAR-bisPSMA treatment by the data cut-off date. Of these six participants, thus far four (66.7%) showed reductions in PSA of 50% or more (PSA50) and two (33.3%) showed reductions of 80% or more (PSA80).

The safety profile of ⁶⁷Cu-SAR-bisPSMA remains favourable in the Cohort Expansion, with the majority of related AEs being Grade 1 or 2. The most common related AEs were nausea and lymphopenia (observed in three out of nine participants [33.3%], for each AE). The only AE that was Grade 3 or above was lymphopenia observed in three participants, some of whom had bone metastasis at baseline and/or had received multiple lines of therapy, including taxane and an investigational agent, prior to enrolment in the SECuRE study. There have been no overall renal toxicity or electrocardiogram (ECG) changes observed in these participants. In the combination enzalutamide arm, no new AEs (or worsening of AEs) related to ⁶⁷Cu-SAR-bisPSMA have been observed to date.

Trial participant with no detectable disease after 3 cycles of ⁶⁷Cu-SAR-bisPSMA

One of the participants in the Cohort Expansion was a 64-year-old man with bone metastases and baseline PSA of 5.4 ng/mL prior to entering the SECuRE study. Following his first cycle of ⁶⁷Cu-SAR-bisPSMA, this participant showed a dramatic 95.2% reduction in PSA. He went on to receive 2 more cycles of ⁶⁷Cu-SAR-bisPSMA and achieved undetectable PSA levels. In a follow-up bone scan and CT no metastatic disease was observed. This participant only exhibited mild (Grade 1) related AEs, most of which were gastrointestinal events, with no haematological or renal AEs observed. The participant reported having excellent quality of life following the treatment.

The interim data from this Phase II continues to confirm the favourable safety profile and promising efficacy seen in previous cohorts of the SECuRE trial^[1] and supports the continuation of the trial with the aim to progress to a registrational Phase III study.

Clarity's Executive Chairperson, Dr Alan Taylor, commented, "SAR-bisPSMA continues generating world-class data in both theranostic and diagnostic trials. The combination of the optimised dimer 'bis' structure with the benefits of copper isotopes, enabled by the proprietary sarcophagine technology, is proving to have created a product that is here to challenge the current treatment and diagnostic paradigms in radiopharmaceuticals.

"We have already seen a glimpse of the effects of ⁶⁷Cu-SAR-bisPSMA through our Dose Escalation cohorts with additional and similar data being generated in the Cohort Expansion phase, demonstrating once again excellent efficacy and safety results of ⁶⁷Cu-SAR-bisPSMA.

"All of the participants with evaluable data treated in the Phase II to date have shown declines in PSA, with the majority showing PSA decreases of more than 50% and mostly having only mild or moderate AEs. Most of these patients have been treated with more than 5 systemic treatment regiments and had bone metastasis prior to entering the SECuRE study. Although the number of participants with evaluable data to date is small, it is incredible to see yet another extraordinary case where a patient who had bone metastasis prior to entering the study achieved undetectable PSA following ⁶⁷Cu-SAR-bisPSMA treatment, with no disease observed by anatomical and molecular imaging at the last assessments. This participant only experienced mild, transient AEs, most being gastrointestinal, and has reported having excellent quality of life following the treatment.

"Importantly, the work we have undertaken during the Dose Escalation Phase is now continuing to provide a strong foundation for us as we look ahead at protocol development and dosing for our Phase III clinical trial and commercialisation. As the participant numbers continue to increase with the trial enrollment, we continue to see very promising responses over and over again, giving us more confidence about the future of this product and its potential for commercialisation in metastatic castration-resistant prostate cancer (mCRPC). With three Fast Track Designations for the SAR-bisPSMA product and positive interactions with the US Food and Drug Administration (FDA) to date, we are working towards bringing this agent to clinicians and their patients around the world through the entirety of the prostate cancer journey, from first diagnosis to late-stage disease. All of these indications, being imaging in pre-definitive therapy and biochemical recurrence, as well as therapy in mCRPC, are blockbuster markets individually for prostate-specific membrane antigen (PSMA) targeted products, with an estimated combined market value of approximately US$10-15 billion by 2030. We are committed to continuing the development of this product, aiming to bring improved diagnostic and treatment options for prostate cancer in various stages of their disease."

About the SECuRE trial

The SECuRE trial (NCT04868604)^[2] is a Phase I/IIa theranostic trial for identification and treatment of participants with PSMA-expressing mCRPC using ⁶⁴Cu/⁶⁷Cu-SAR-bisPSMA. ⁶⁴Cu-SAR-bisPSMA is used to visualise PSMA-expressing lesions and select candidates for subsequent ⁶⁷Cu-SAR-bisPSMA therapy. The trial is a multi-centre, single arm, dose escalation study with a cohort expansion involving approximately 54 participants in the US. The overall aim of the trial is to determine the safety and efficacy of ⁶⁷Cu-SAR-bisPSMA for the treatment of prostate cancer.

The SECuRE trial consists of the Dose Escalation (Phase I) and Cohort Expansion (Phase II) Phases. Based on the data from the Dose Escalation Phase, which demonstrated a favourable safety profile and efficacy of ⁶⁷Cu-SAR-bisPSMA, the SECuRE trial progressed to the Cohort Expansion (Phase II) at an 8 GBq dose level as per the SRC recommendation (up to 6 cycles per patient in total)^[3].

Cohort 2 of the Dose Escalation phase of the trial, where participants were dosed with 8 GBq of ⁶⁷Cu-SAR-bisPSMA, demonstrated a very low rate of related AEs while all three participants achieved PSA declines of 80% or more (PSA80)^[1]. The Dose Escalation Phase also showed high PSA response rates of the mCRPC in the pre-chemotherapy setting with a favourable safety profile: 92% of pre-chemotherapy participants (12/13) demonstrated PSA drops greater than 35%, PSA reductions greater than 50% were reached in 61.5% (8/13) of participants, and reductions of 80% or more were achieved in 46.2% (6/13) of participants^[1]. These results supported the progress of the trial to its Cohort Expansion Phase using 8 GBq multi-dose in participants who had not received chemotherapy in the mCRPC setting.

Recruitment is currently ongoing into the Cohort Expansion Phase which will include 24 participants. A subset of participants will be treated with the combination of 8 GBq of ⁶⁷Cu-SAR-bisPSMA with enzalutamide (androgen receptor pathway inhibitor [ARPI]), in line with the positive results from the Enza-p trial^[4] and previous discussions with and advice from key global medical experts in the field of prostate cancer, including the Company's Clinical Advisory Board members, Prof Louise Emmett and Prof Oliver Sartor, as well as the SRC.

About SAR-bisPSMA

SAR-bisPSMA derives its name from the word "bis", which reflects a novel approach of connecting two PSMA-targeting agents to Clarity's proprietary sarcophagine (SAR) technology that securely holds copper isotopes inside a cage-like structure, called a chelator. Unlike other commercially available chelators, the SAR technology prevents copper leakage into the body. SAR-bisPSMA is a Targeted Copper Theranostic (TCT) that can be used with isotopes of copper-64 (Cu-64 or ⁶⁴Cu) for imaging and copper-67 (Cu-67 or ⁶⁷Cu) for therapy.

⁶⁷Cu-SAR-bisPSMA and ⁶⁴Cu-SAR-bisPSMA are unregistered products. The safety and efficacy of ⁶⁷Cu-SAR-bisPSMA and ⁶⁴Cu-SAR-bisPSMA have not been assessed by health authorities such as the US FDA or the Therapeutic Goods Administration (TGA). There is no guarantee that these products will become commercially available.

About Prostate Cancer

Prostate cancer is the second most common cancer diagnosed in men globally and the fifth leading cause of cancer death in men worldwide^[5]. Prostate cancer is the second-leading causes of cancer death in American men. The American Cancer Institute estimates in 2025 there will be about 313,780 new cases of prostate cancer in the US and around 35,770 deaths from the disease^[6].

About Clarity Pharmaceuticals

Clarity is a clinical stage radiopharmaceutical company focused on the treatment of serious diseases. The Company is a leader in innovative radiopharmaceuticals, developing TCTs based on its SAR Technology Platform for the treatment of cancers.

www.claritypharmaceuticals.com

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