Business Wire

Blue Planet Science Fiction Film Festival Highlighted at the 77th Venice Film Festival

Share

China’s Blue Planet Science-Fiction Film Festival was highlighted at the 77th Venice International Film Festival during the “Focus on China” side event earlier this week, bringing a glimpse of the future to the world’s oldest film festival.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20200908005606/en/

To view this piece of content from mms.businesswire.com, please give your consent at the top of this page.

Blue Planet Sci-Fi Film Festival presented at "Focus on China" event during Venice International Film Festival (Photo: Xinhuanet)

The Venice International Film Festival is one of the first major cultural events held in Europe since the outbreak of the COVID-19 pandemic. The fact that the festival - one of the film industry’s most important annual events - could go ahead offline as planned is a major boost to a sector that has been hit hard by the pandemic. The “Focus on China” event was held in the National Pavilion of Italy and streamed online.

2019 was an international breakthrough year for Chinese sci-fi cinema. November 2019 saw the inaugural Blue Planet Sci-Fi Film Festival, the first of its kind in China. It recorded great success, with 185 sci-fi films from 17 countries screened and a series of activities such as forums, masterclasses and exhibitions held.

The second Blue Planet Sci-Fi Film Festival will be held in November 2020. In light of the difficult times our world is going through, the theme of this year’s festival will be “empathy”. “Amidst this global crisis, it is more important than ever for people around the world to transcend barriers and engage with each other,” said the Blue Planet Organizing Committee in a message to the event.

Industry figures at the Venice Film Festival noted a buzz around the development of Chinese sci-fi. Roberto Stabile, head of international relations for the Italian motion picture association ANICA, said, “I was very impressed by this introduction to the Blue Planet Sci-Fi Film Festival, and look forward to welcoming our friends from the Blue Planet in Venice next year.”

Italian-Chinese filmmaker Shi Yangshi said, “Two years ago, Italian director Giuseppe Tornatore talked to me about Liu Cixin’s sci-fi novels and showed great interest in co-producing sci-fi films with China.” Italian producer Luca Confortini remarked, “China has a well-established film culture and its sci-fi films have been developing rapidly. The Blue Planet is an important and vibrant film event; I believe that China’s sci-fi film market will only grow bigger.”

Six Chinese-directed sci-fi short films chosen from the first Blue Planet were screened during the Film Festival.

To view this piece of content from cts.businesswire.com, please give your consent at the top of this page.

Contact information

Xinhuanet Europe
Wei Wang
info@xinhuaeurope.com

About Business Wire

For more than 50 years, Business Wire has been the global leader in press release distribution and regulatory disclosure.

Subscribe to releases from Business Wire

Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from Business Wire

BeOne Medicines Granted U.S. FDA Fast Track Designation for BGB-B2033 as Treatment for Hepatocellular Carcinoma18.12.2025 13:00:00 EET | Press release

BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced that the U.S. Food and Drug Administration (FDA) has granted the Company Fast Track Designation for BGB-B2033, its GPC3x4-1BB bispecific antibody for the treatment of adult patients with hepatocellular carcinoma (HCC) with disease progression on or after prior systemic treatment. “The FDA awards Fast Track Designation to therapies that show potential to address an unmet medical need in serious or life-threatening conditions. The FDA’s decision reflects the encouraging profile of BGB-B2033 in advanced hepatocellular carcinoma, where patients continue to face limited treatment options,” said Julie Lepin, Senior Vice President and Chief Regulatory Affairs Officer at BeOne. BeOne is currently conducting a global, multi-center Phase 1 clinical trial (NCT06427941) to explore the safety and anti-tumor activity of BGB-B2033, both alone and in combination with PD-1 inhibitor TEVIMBRA® (tisle

NHOA Energy Achieves Great Place To Work Certification in Italy, the United States and Australia18.12.2025 11:53:00 EET | Press release

NHOA Energy, global provider of utility-scale energy storage systems, announces that it has been certified Great Place To Work® in Italy, the United States, and Australia. The certification is based entirely on direct feedback from NHOA Energy employees, gathered through an independent and structured listening process. Great Place To Work® Certification™ assesses the quality of the employee experience across key dimensions such as credibility, respect, fairness, pride, and camaraderie. The results achieved by NHOA Energy reflect a corporate culture built on trust, inclusion, and the consistent commitment to valuing people within a dynamic and international environment. Employees highlighted particularly high levels of appreciation for the ethical and transparent behavior of leaders, the welcoming and inclusive approach toward new hires, and fair treatment across diversity, equity, and inclusion dimensions. A strong majority also expressed pride in working at NHOA Energy and reported a

Regnology Signs an Agreement to Acquire Moody’s Regulatory Reporting & ALM Solutions18.12.2025 11:00:00 EET | Press release

Regnology, a leading provider in regulatory, risk, tax, and finance reporting, as well as supervisory technology, today announced it has signed an exclusive agreement for the acquisition of Moody’s Regulatory Reporting & ALM Solutions business, inclusive of solutions for Basel III compliance, IFRS9 impairment accounting, large bank asset-liability management (ALM), Solvency II insurance reporting, and prudential and statistical regulatory reporting across more than 50 jurisdictions. By integrating Moody’s regulatory capital and liquidity capabilities with Regnology’s regulatory, risk, and finance offerings, the firm is creating a unified, scalable platform designed to meet the full spectrum of financial regulatory compliance and risk requirements. This combined strength positions Regnology as the partner of choice for financial institutions seeking future-ready solutions. At the core of this strategy is Regnology Risk Hub (RRiskHub), an integrated solution designed to deliver a single

Reply Recognized as a Microsoft Azure Expert Managed Services Provider for the Sixth Consecutive Year18.12.2025 11:00:00 EET | Press release

Reply [EXM, STAR: REY] announced today it has been recognized once again as a Microsoft Azure Expert Managed Services Provider (MSP). The renewal reaffirms Reply’s proven expertise and consistent track record in delivering high-quality cloud solutions and services on the Microsoft Azure platform, powered by the deep technical expertise of its specialized companies – Cluster Reply, Solidsoft Reply and Valorem Reply. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20251218596617/en/ This recognition reflects the ongoing collaboration between Reply - through its companies Cluster Reply, Solidsoft Reply, and Valorem Reply - and Microsoft, supporting shared efforts to deliver value-driven services to enterprise customers. The Azure Expert MSP program is designed by Microsoft to identify and validate partners with proven capabilities in delivering end-to-end Azure services at scale. To qualify, partners must meet a strict set of requ

Takeda’s Zasocitinib Landmark Phase 3 Plaque Psoriasis Data Show Promise to Deliver Clear Skin in a Once-Daily Pill, Catalyzing a New Era of Treatment18.12.2025 10:00:00 EET | Press release

Takeda(TSE:4502/NYSE:TAK)today announced positive topline results for the two pivotal Phase 3randomized, multicenter, double-blind, placebo- and active comparator-controlled studies of zasocitinib (TAK-279), a next-generation, highly selective oral tyrosine kinase 2 (TYK2) inhibitor, in adults with moderate-to-severe plaque psoriasis (PsO). The studies demonstrated superiority of zasocitinib compared to placebo for the co-primary endpoints, static Physician Global Assessment (sPGA) 0/1 and Psoriasis Area and Severity Index (PASI) 75, at week 16, with a significantly greater PASI 75 response rate seen as early as week 4 and continuing to increase through week 24. The studies also met all 44 ranked secondary endpoints, including PASI 90, PASI 100 and sPGA 0 against placebo and apremilast, showing the potential of a convenient once-daily pill to deliver complete skin clearance for patients with PsO. “People living with psoriasis continue to seek safe, effective and fast-acting oral therap

In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.

Visit our pressroom
World GlobeA line styled icon from Orion Icon Library.HiddenA line styled icon from Orion Icon Library.Eye