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Babson Capital Corporate Investors

20.58

-0.2100-1.01%

Post-market: 20.580.00000.00%16:10 EST

Volume:27.34K

Turnover:563.89K

Market Cap:421.86M

PE:13.18

High:20.86

Open:20.62

Low:20.51

Close:20.79

52wk High:25.24

52wk Low:18.60

Shares:20.50M

Float Shares:- -

Volume Ratio:2.01

T/O Rate:- -

Dividend:1.70

Dividend Rate:8.26%

EPS(TTM):1.56

EPS(LYR):1.74

ROE:9.13%

ROA:5.63%

PB:1.21

PE(LYR):11.80

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Overview Company News Filings

Eisai Presents New Data on the Continued and Expanding Benefit of LEQEMBI® (lecanemab-irmb) Maintenance Treatment in Early Alzheimer’s Disease at the Clinical Trials on Alzheimer’s Disease (CTAD) Conference 2025

New Data Presented at the Clinical Trials on Alzheimer’s Disease (CTAD) Conference 2025 Confirms Pharmacological Effect of LEQEMBI® (lecanemab-irmb) on Neurotoxic Aβ Protofibrils in CSF

Eisai Submits New Drug Application for Subcutaneous Formulation of “LEQEMBI®” for the Treatment of Early Alzheimer’s Disease in Japan

Eisai Completes Rolling Submission to US FDA for LEQEMBI® IQLIK™ (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer’s Disease Under Fast Track Status

“LEQEMBI®” (lecanemab) IV Maintenance Dosing for the Treatment of Early Alzheimer’s Disease Approved in the United Kingdom

Barings Corporate Investors reports Q3 net investment income of $7.1 million

Nexalin Technology’s Q-Submission for Gen-2 SYNC Accepted by U.S. FDA for the Treatment of Alzheimer’s Disease and Dementia

India Inflation Cools Further in September

MT Newswires Live

LEQEMBI® IQLIK™(lecanemab-irmb) Subcutaneous Autoinjector Named to TIME’s “Best Inventions of 2025”

LEQEMBI® (Lecanemab) Approved for the Treatment of Alzheimer’s Disease in Australia

How a new three-minute memory test can help spot Alzheimer's disease

Cognition Therapeutics Study of Zervimesine (CT1812) in Early Alzheimer’s Disease Reaches 75% Enrollment Target

Eisai Initiated Rolling Supplemental Biologics License Application to the U.S. FDA for LEQEMBI® IQLIK™ (lecanemab-irmb) as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer’s Disease Under Fast Track Status

FDA Approves LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection for Maintenance Dosing for the Treatment of Early Alzheimer's Disease

Austria and Germany to become the first markets in the European Union (EU) to launch LEQEMBI® (lecanemab)

Barings Corporate Investors Q2 Dividend USD 0.4

THOMSON REUTERS

Press Release: Barings Corporate Investors Reports Preliminary Second Quarter 2025 Results and Announces Quarterly Cash Dividend Of $0.40 Per Share

India Wholesale Price Index Deflation Deepens in July

MT Newswires Live

Two-Year Real-World Study of LEQEMBI® in the United States Presented at Alzheimer's Association International Conference (AAIC) 2025

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June 30, 2025 figures net of less than $0.01 per share of excise tax.     June 30, 2025 figures net of less than $0.01 per share of capital gains.     Based on shares outstanding at the end of the period of 20,444,621. The Board of Trustees declared a quarterly dividend of $0.40 per share, payable on September 12, 2025, to shareholders of record on August 29, 2025.During the three months ended June 30, 2025, the Trust reported total investment income of $9.3 million, net investment income of $7.2 million, or $0.35 per share, and a net increase in net assets resulting from operations of $8.8 million, or $0.43 per share.Net asset value  per share as of June 30, 2025, was $17.10, as compared to $17.07 as of March 31, 2024. 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