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Brookfield Real Assets Income Fund Inc.

12.53

+0.02000.16%

Post-market: 12.530.00000.00%16:15 EDT

Volume:117.86K

Turnover:1.48M

Market Cap:692.34M

PE:10.62

High:12.55

Open:12.55

Low:12.51

Close:12.51

52wk High:13.59

52wk Low:12.50

Shares:55.25M

Float Shares:55.25M

Volume Ratio:0.76

T/O Rate:0.21%

Dividend:1.42

Dividend Rate:11.30%

EPS(TTM):1.18

ROE:--

ROA:--

PB:0.87

PE(LYR):- -

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Overview Company News Filings

Artiva Biotherapeutics to Participate in Upcoming Investor Conferences in September

Priovant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults with Dermatomyositis; Now Available in the U.S.

Spyre Therapeutics announces results from RA sub-study of SKYWAY basket trial

Spyre Therapeutics Announces Topline Results from the Rheumatoid Arthritis Sub-study of the SKYWAY Phase 2 Trial of SPY072

Chemomab Therapeutics Announces Second Quarter 2026 Financial Results and Provides Corporate Update

Press Release: First Tracks Biotherapeutics Announces Second Quarter 2026 Financial Results and Provides Business Update

Press Release: Vor Bio Reports Second Quarter 2026 Financial Results and Provides Corporate Update

Heron Therapeutics Announces Second Quarter 2026 Financial Results

Artiva Therapeutics: Buy Rating Reiterated on Strong AlloNK RA Profile and Upcoming Phase III, Price Target Maintained at $41

Artiva Biotherapeutics Reports Second Quarter 2026 Financial Results and Recent Business Highlights

Press Release: Cullinan Therapeutics Provides Corporate Update and Reports Second Quarter 2026 Financial Results

Federal Jury Rules Avilar and RA Capital Guilty of Willfully Misusing Yale University's Trade Secrets

Biohaven Awarded $1 Million Over Alleged Trade Secret Violations by Avilar Therapeutics, RA Capital Management

MT Newswires Live

Artiva Biotherapeutics Announces New Employee Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

Chemomab Therapeutics and Precision Medicine Pioneer Scipher Medicine Announce Merger Agreement to Advance Nebokitug in an AI-Powered Phase 2 Trial in Rheumatoid Arthritis

Press Release: Vor Bio Appoints David Zaccardelli to Board of Directors

Brookfield Real Assets Income Fund Declares Q3 Monthly Distribution of $0.118 Per Share

SynAct’s RA Drug Resomelagon Delivers Positive Phase 2b Data, Fuels Partnering Push

FREELANDER 8 Makes First Public Appearance Ahead of Official Abu Dhabi Launch

SynAct extends U.S. patent exclusivity for lead RA therapy resomelagon to 2044

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top-line Cohort 1 data reaffirmed for Q4. -- Cohort 2  enhanced to enroll up to 40 patients including. those with a broad range of histologic  and symptom. severity to further inform future development; top-line Cohort 2 data. -- U.S. FDA granted Fast Track designation for ANB033 for the treatment of. -- Enrollment ongoing for Phase 1b ANB033 trial in eosinophilic esophagitis. -- Reiterating cash-runway into Q2 2028, including the expansion of ANB033. -- U.S. FDA granted Fast Track designation to ANB033 for the. treatment of people with CeD on a gluten-free diet. -- 70-patient trial assessing one dose level of subcutaneously. -- Cohort 1  is a gluten-challenge study to assess the. -- Cohort 2  assesses the possibility of mucosal healing","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","SLE","RA","BK4077","TRAX"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2658915593","title":"Press Release: Vor Bio Reports Second Quarter 2026 Financial Results and Provides Corporate Update","url":"https://stock-news.laohu8.com/highlight/detail?id=2658915593","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2658915593?lang=en_us&edition=fundamental","pubTime":"2026-08-11 21:30","pubTimestamp":1786455000,"startTime":"0","endTime":"0","summary":"placebo-controlled Phase 3 registrational trial with an open-label. extension assessing the efficacy and safety of telitacicept in gMG. -- Topline data anticipated in 1H 2027Primary Sjgren's Disease-- UPSTREAM SjD. efficacy and safety of telitacicept in SjDCorporate Updates-- Appointed David Zaccardelli, Pharm.D., former Chief Executive Officer and. 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