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Industrial Minerals Ltd

0.105

+0.0066.06%

Volume:121.71K

Turnover:12.78K

Market Cap:17.08M

PE:-12.80

High:0.105

Open:0.102

Low:0.102

Close:0.099

52wk High:0.200

52wk Low:0.092

Shares:162.69M

Float Shares:117.64M

Volume Ratio:1.72

T/O Rate:0.10%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-0.008

EPS(LYR):-0.008

ROE:-19.12%

ROA:-9.97%

PB:4.09

PE(LYR):-12.80

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Overview Company News Filings

Australia's Industrial Minerals Jumps After Securing Exploration Licence for Gold Project

Industrial Minerals Ltd-North Pool Tenement Granted

THOMSON REUTERS

Kringle Pharma Submits IND Application for Spinal Cord Injury Drug to U.S. FDA; Shares Jump 7%

MT Newswires Live

Industrial Minerals Ltd-Appendix 4G & Corporate Governance Statement

THOMSON REUTERS

Celltrion Secures IND Application Amendment Approvals for CT-P44, CT-P51 Phase 3 Trial

MT Newswires Live

Industrial Minerals Ltd-Change in Substantial Holding X2

THOMSON REUTERS

Industrial Minerals Ltd-S708a Cleansing Notice

THOMSON REUTERS

Industrial Minerals Ltd-Application for Quotation of Securities - Ind

THOMSON REUTERS

Industrial Minerals - Jeffrey Sweet Steps Down as Managing Director, Continues as Non-Executive Director

THOMSON REUTERS

Industrial Minerals Ltd-Completion of Galleon Metals Acquisition & Board Changes

THOMSON REUTERS

Industrial Minerals Ltd-Geophysics Confirms Strong Gold Target at Laverton

THOMSON REUTERS

Industrial Minerals Ltd-Results of Meeting

THOMSON REUTERS

Trump: University of Miami donates 1994 Ibogaine IND to accelerate treatment for veterans

Trump's Truth Social latest posts

Caliway Biopharma Submits China Phase 1 IND for CBL-514 Fat-Reduction Drug

MT Newswires Live

Celltrion Submits Dual-Part EMA Application for Subcutaneous Rheumatoid Arthritis Drug

MT Newswires Live

Celltrion Submits Amendment for Phase 3 Trial of Cancer Biosimilar to US FDA

MT Newswires Live

BUZZ-Australia's Industrial Minerals jumps on onshore gold find

Industrial Minerals Ltd-High-Grade Historic Gold Results Confirmed at Laverton

THOMSON REUTERS

Antengene Secures China IND Approval for Autoimmune Disease Drug

MT Newswires Live

Telix Pharmaceuticals Says Prostate Cancer Treatement Candidate Shows Acceptable Tolerability in Phase Three Trial

MT Newswires Live

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Social latest posts","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2660949985?lang=en_us&edition=fundamental","pubTime":"2026-08-19 00:57","pubTimestamp":1787072260,"startTime":"0","endTime":"0","summary":"President Donald Trump announced on August 18 that the University of Miami has donated its original 1994 Ibogaine Investigational New Drug (IND) application to the federal government, a move he said...","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://trumpstruth.org/statuses/40964","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":["IND.AU","IND","BK7095"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2656261587","title":"Caliway Biopharma Submits China Phase 1 IND for CBL-514 Fat-Reduction Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2656261587","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2656261587?lang=en_us&edition=fundamental","pubTime":"2026-08-04 14:19","pubTimestamp":1785824364,"startTime":"0","endTime":"0","summary":"Caliway Biopharmaceuticals  submitted an investigational new drug  application to China's National Medical Products Administration's Center for Drug Evaluation for a phase one study of abdominal fact reduction drug.The CBL-0102 trial will evaluate the safety, tolerability and pharmacokinetic profile of CBL-514 in about 30 healthy Chinese subjects, following completion of a pre-IND meeting with the regulator.The company said the localized phase 1 study will assess potential racial differences in the drug's efficacy and safety between Chinese and non-Chinese populations, with a China phase 3 application planned after the phase 1 study is completed.","market":"us","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://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["IND","BK7095","IND.AU","CBL","BK4080","BK4231"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2653088115","title":"Celltrion Submits Dual-Part EMA Application for Subcutaneous Rheumatoid Arthritis Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2653088115","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2653088115?lang=en_us&edition=fundamental","pubTime":"2026-07-24 17:23","pubTimestamp":1784885030,"startTime":"0","endTime":"0","summary":"Celltrion  has submitted applications for its subcutaneous rheumatoid arthritis drug CT-P13 SC  to both the U.S. FDA  and the European Medicines Agency .The company seeks to demonstrate superiority over placebo at 12 weeks in a 296-patient, 52-week global Phase 3 trial, according to a bourse filing on Friday.The subcutaneous formulation, already approved for ulcerative colitis and Crohn's disease in multiple regions, aims to expand its indications and improve patient convenience through a broader treatment population.The company cautions that historically only about 10% of clinical trial drugs ultimately receive marketing approval, and results may fall short of expectations.While both filings share the same clinical design and commercial rationale, the EMA submission explicitly addresses the EU's revised Clinical Trials Regulation requiring separate Part 1  and Part 2  approvals.Both submissions support commercial differentiation through patient diversity, though investors are urged 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investigational new drug  amendment for a global Phase 3 trial of CT-P51, the biosimilar of its cancer drug Keytruda, to the U.S. Food & Drug Administration, according to a Monday filing with the Korea Exchange.The randomized, double-blind, active-controlled clinical trial will enroll 220 previously untreated patients who have metastatic non-squamous non-small cell lung cancer to compare the efficacy and safety of CT-P51 against the reference drug over a two-year treatment period, the filing 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