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1The new U.S. earnings season kicks off this week: U.S.-Iran negotiations break down, can bank giants' earnings boost market sentiment?2Oil Surpasses $100 After U.S. Navy Closes Strait of Hormuz - How Serious Is the Threat to Supply?

Johnson Controls JCI Jumps 4.39% to $139 as Trading Volume Signals Bullish Turnaround
101 finance·2026/04/09 03:15

Applovin Shares Tumble 4.69% as Technicals Signal Deeper Correction
101 finance·2026/04/09 03:15
BBGIs Earnings Tank, Yet Shares Spike on Debt Restructuring
101 finance·2026/04/09 03:12

TUTUSDC Rallies on Surging Volume, Then Falters as Sellers Reclaim Control
101 finance·2026/04/09 03:12

Oracle’s $553 Billion AI Pipeline: Does the Stock Reflect Potential Execution Challenges or Anticipated Rewards?
101 finance·2026/04/09 03:09

Comcast's April 23 Financial Results May Change the Story Around Broadband Customer Losses
101 finance·2026/04/09 03:09

Aehr Test Systems Misses Earnings, Yet Stock Hits All-Time High
101 finance·2026/04/09 03:06

Viking Soars 8.97% on Volume Surge as Technical Breakout Confirms Bullish Trend
101 finance·2026/04/09 03:06

Anthropic's Mythos Leak: A Cybersecurity Stock Repricing Event
101 finance·2026/04/09 02:57

Wells Fargo Acts as a Steadying Force in the U.S. Repo Market as Analysts Differ
101 finance·2026/04/09 02:54
Flash
08:57
UBS lowers ServiceNow target price to $100GLONGHUI April 13|UBS has lowered ServiceNow's target price from $170 to $100 and downgraded its rating from "Buy" to "Neutral". (GLONGHUI)
08:48
US Stock Movement | Replimune plunges over 56% in pre-market trading as RP1's listing application is rejected by the FDA againGlonghui, April 13 — Biotechnology company Replimune (REPL.US) fell more than 56% to $2.09 before market open. According to reports, Replimune’s core drug RP1 failed to obtain FDA approval. On April 10, 2026, the FDA issued a Complete Response Letter (CRL), officially rejecting the drug’s marketing application. The FDA rejected the RP1 application once again, citing insufficient clinical trial design and data inadequate to support its efficacy. Although the drug itself showed decent efficacy and safety data, the FDA has set stricter evidence standards for the “accelerated approval” pathway. This marks the second major setback for RP1 since its first rejection in July 2025.
08:44
Have Chinese companies obtained lithium export qualifications in Zimbabwe? Chengxin Lithium respondsGolden Ten Data, April 13 — Recently, market sources reported that lithium mine exports in Zimbabwe have shown signs of easing, and currently, several Chinese-funded enterprises have already obtained export qualifications; the specific quota is expected to be announced soon. In response, a staff member from Shengxin Lithium Energy confirmed today that the company’s local team has been in communication with Zimbabwean government departments. Although they did not explicitly mention having obtained the export license, they stated that “there has been substantial progress now” and “as soon as they grant the quota, exports may happen very soon. There were no specific implementation details before.” The staff member added that, although the specific quota figures are not yet known, “the export volume we require will be sufficient.”
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